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NR449 Mod4 Nov24

39:32EnglishTranscribed Jul 27, 2026
0:02

hey everybody so let's talk this week

0:04

about sampling strategy to begin with

0:08

beginning with chapter seven in your

0:10

book it's also very well outlined in

0:13

your edep I hope you're paying attention

0:14

to that

0:16

okay so we're going to be talking about

0:18

sampling strategies sampling error and a

0:21

lot you know we talked we got into the

0:24

conversation last week about qualitative

0:27

versus quantitative data and so we're

0:30

going to continue on with qualitative

0:32

and quantitative research looking at

0:35

differences and comparing and whatnot

0:38

and so let's get

0:42

started one of the things that you

0:44

always need to be concerned about with

0:46

with research is bias bias of your own

0:51

bias the way the study is laid out

0:53

there's a lot of different ways to to

0:55

look for to have

0:57

bias one of the ways is we pick our

1:00

subjects based on how we think they're

1:03

going to respond I want to know that my

1:07

research that my way of doing things is

1:09

better than the old way so I may pick my

1:12

sample based on how I think they're

1:14

going to respond and not randomly or

1:17

impartially so I've biased my results

1:20

and they may not be

1:21

right which is going to threaten the

1:24

validity of the study certainly going to

1:26

uh affect the usability of the study we

1:30

control that like I said through random

1:32

sampling random assignment to groups so

1:35

if I have a group of a

1:39

thousand people that have

1:43

cancer and I decide that I want a sample

1:46

of 500 so I will throw a thousand names

1:50

in the head and I'll pull out until I

1:51

have my 500 randomly decided randomly

1:55

chosen I pulled out 500 I could use a

1:58

table of random numbers and do the same

2:00

thing where I could put everybody's

2:02

number give everybody a number and then

2:05

pull numbers randomly until I have 500

2:08

so once I've done that then I take my

2:11

500 and I'll randomly assign them to a

2:15

group as well so maybe I'm looking at

2:18

two different things and I will randomly

2:20

decide who goes to which group maybe

2:22

this is the control group and this is

2:25

the group that actually has is going to

2:27

get the treatment we did that with study

2:30

of single cell patients when we started

2:32

penicillin prophylaxis we wanted to know

2:35

in our children if penicillin

2:37

prophylaxis would prevent death would

2:40

prevent hospitalization and serious

2:42

complications of infection and so we

2:44

started a study and we put everybody

2:49

when they came to Clinic they were asked

2:51

to participate and then those that

2:53

participated were randomly assigned to

2:57

either the treatment group they got

3:00

penicillin or to the control group and

3:04

they got vitamin C neither the patient

3:08

nor the physician nor the nurses knew

3:13

what that patient was getting so we

3:16

didn't know whether they had penicillin

3:18

or not and that's called Blind we did

3:21

blindly assign them to groups

3:27

randomly sampling size

3:30

it is really what you're looking at to

3:32

determine that you have enough subjects

3:34

from that

3:36

population to get valid results to get

3:39

quality results two

3:42

people all the subjects agreed right but

3:45

you only had

3:48

two I have a thousand and 980 agreed now

3:52

you've got much more data to go with

3:54

right so you want it to represent the

3:57

population too you don't want to pick

3:58

and choose that bias

4:00

but you want to have a group when you're

4:02

done of participants that really reflect

4:05

what's out

4:09

there so how do you choose them well

4:12

first of all you define that population

4:15

Define exactly what you want maybe

4:17

patients between the age of 20 and 40

4:20

who have type 2

4:25

diabetes we could say they're overweight

4:27

or not you could give you could take a a

4:31

gender or not but Define that population

4:35

that you want to do and then look at

4:39

those members of the population who are

4:41

attainable your sampling frame who do

4:44

you have access

4:46

to finally look at inclusion and

4:49

exclusion criteria we're going to talk a

4:51

little more about that but who are you

4:53

going to include and who are you going

4:54

to exclude it's really important and why

4:57

do you exclude some is that going to buy

5:00

us your study

5:05

then so inclusion and exclusion criteria

5:09

really are the demographics maybe what

5:12

are we going to

5:14

include children between the age of five

5:17

and 10 who live in a certain area who

5:22

are able to read and write and complete

5:24

the questionnaire who have their parents

5:27

consent who come to clinic on these days

5:30

all of those things that you're going to

5:32

include right exclusion criteria then

5:35

for that study would be they can't read

5:38

and

5:39

write they didn't come to clinic on the

5:41

same day if they had another condition

5:44

maybe maybe I'm looking at people 5 to

5:46

10 years old who have acute lymphatic

5:49

leukemia but let's say that this patient

5:52

also had congenital heart

5:54

disease are they also have Down syndrome

5:58

am I going to include those then that

6:01

may be an exclusion

6:05

criteria sometimes there are behavioral

6:07

factors that might pose a risk for a

6:10

high attrition rate and we want to avoid

6:14

those I don't know some kind of study

6:16

where you were looking at somebody with

6:18

ADHD and they might not be as likely to

6:21

continue on the study like you want them

6:23

to or might not agree to complete the

6:25

questionnaire once they start something

6:28

like that so you're looking at anything

6:30

that's going to help to control

6:33

extraneous variables that might

6:36

unintentionally impact your

6:41

results sampling in studies qualitative

6:44

and

6:45

quantitative qualitative you know we're

6:48

going to keep comparing these that

6:50

purposeful selection it's not random

6:53

right we need the people who we think

6:58

are going to best be be able to sit down

7:02

with us for an hour or two hours and

7:04

have a conversation about the

7:08

topic maybe it's a study of why people

7:14

smoke right so number one you've got to

7:17

have somebody who smokes somebody who's

7:20

willing to sit down and talk and let you

7:23

know what's going

7:26

on and for that reason you're looking at

7:29

that you're you're looking at a fairly

7:32

homogeneous group probably right you're

7:35

looking at somebody's very purposefully

7:37

chosen because they have the

7:41

qualifications that you

7:44

need quantitative on the other hand may

7:46

use probability sampling or random

7:48

sampling you know and that's what I

7:50

talked about with our children with

7:52

sickle cell no we didn't randomly choose

7:55

from the greater population we took

7:58

everybody

8:00

that would agree every patient that we

8:03

had that had CLE cell they were under

8:05

the age of six um and they agreed we

8:08

signed them up we could have just as

8:10

easily said look we have a thousand

8:12

patients we're going to choose randomly

8:15

500 and then from those 500 we're going

8:18

to randomly assign somebody to get

8:21

penicillin and somebody to get the

8:23

placebo

8:26

random essentially every member of the

8:30

population when you're doing random

8:32

sampling has an equal probability of

8:34

being selected so we while we took

8:38

everybody that was in that

8:41

population once they were on the study

8:44

they all had an equal probability of

8:47

getting either the the study drug or the

8:51

placebo and then every subject selection

8:55

is

8:56

independent doesn't depend on who just

8:59

just we don't say okay well we just took

9:01

three that are getting penicillin so our

9:04

next one is going to be we don't do that

9:07

again it gets thrown in a hat tossed

9:09

around pull out a

9:16

number this is what I was saying before

9:18

a table of random

9:23

numbers whoops sorry um a table of

9:26

random numbers requires access to a list

9:28

of population members systematic random

9:32

sampling is a random selection of a

9:35

starting point let's say that we give

9:37

everybody a number and we just randomly

9:42

pick numbers you can close your eyes and

9:43

put your finger on a table that's number

9:46

79 we'll take 79 close your eyes and

9:48

touch it again you're just going to get

9:51

a list and you're going to randomly

9:52

choose systematic random is a little

9:56

more different in that let's say that we

9:58

have a list of subjects and we're going

10:00

to choose every fifth one so we'll count

10:05

1 2 3 4 five we'll take number five 1 2

10:08

3 4 5 we'll take number 10 1 2 3 4 5

10:11

number 15 and we'll keep going until

10:13

we've gone through our list taking every

10:16

fifth

10:18

subject stratified random sampling is

10:21

drawn from stratifications based on some

10:24

characteristic that you're interested in

10:26

we'll use that to do our sampling

10:30

cluster random sampling

10:32

is essentially a random selection of

10:35

entire

10:37

groups and that cluster then we measure

10:41

everybody in it everybody in the group

10:43

gets measured they're are

10:49

cluster ensuring Independence we want to

10:53

be sure that every set of data every

10:56

person is independent they're

10:58

independently chosen

11:00

right if somebody is related if they're

11:02

related in some way if you have a bias

11:05

and you choose certain patients

11:08

then you violate that Independence if

11:12

you get more than one score well oh this

11:15

one I like better so I'm going to take

11:16

it versus the first one they did you

11:19

violate that at

11:21

Independence so pretest and protest is

11:24

not independent right you've got you do

11:26

a test you do some intervention and then

11:31

you test again or time series because

11:34

they've already had a

11:37

score and an intervention and they're

11:39

doing it again you see how that's not

11:43

hopefully not

11:45

independent has good qualities and

11:48

sometimes we want to do that but there

11:50

you go the most common thing we do

11:53

honestly is convenience

11:55

sampling I had to do that to get through

11:58

with my dis

12:00

dissertation it is where you take

12:04

whoever subjects are available in a

12:07

convenient way to the researcher I went

12:09

to clinic I asked every child that

12:11

showed up to Clinic that day if they

12:14

would participate it took forever to get

12:18

subjects I will say and I really thought

12:20

it wouldn't take us long I one time I

12:22

decided to go to camp and I got kids who

12:24

were coming and checking in at camp with

12:26

their parents and I got them to sit down

12:28

with me and do my questionnaires really

12:30

quickly so that was one way to do it uh

12:33

snowball sampling is convenience

12:35

sampling too and that maybe I have a

12:38

subject and they've done my

12:41

questionnaire um um maybe it's somebody

12:44

who knows other people if you're looking

12:52

at somebody who's homeless they know

12:55

other homeless

12:56

people maybe they'll recruit them for

12:58

you maybe I want to look at cheerleaders

13:01

and so I have a subject who's a

13:03

cheerleader and she can recruit or he

13:05

can recruit other subjects in that meet

13:09

those qualifications it decreases your

13:11

generalizability because of that but

13:14

often times we can get what we need in

13:17

that way convenience sampling quite

13:19

often is used in a pilot study or a

13:23

study to find out if we can even do the

13:25

study you kind of test everything out to

13:28

see if it works

13:30

random assignment then can be done on

13:33

top of convenience sampling and I guess

13:36

that's kind of what you could say we did

13:37

in that we took everybody who came to

13:39

Clinic which is

13:41

everybody and then from that we randomly

13:44

assigned them to the two groups and that

13:47

helped with bias we weren't choosing who

13:49

got study medicine and who didn't and we

13:51

didn't know who got study medicine and

13:53

who didn't

13:57

so uh hard to reach populations you can

14:01

speak in their native tongue if you know

14:05

the language you can use experience

14:08

sampling methods respondent driven

14:11

sampling people who will participate

14:14

people who will complete a questionnaire

14:16

or send it to you service based sampling

14:19

out there is a well is an opportunity to

14:22

get hard to reach

14:24

areas we can do mixed methods and that's

14:27

when maybe we're studying something very

14:30

rare rare

14:31

disease um or disaster responses we got

14:35

a lot of those lately right um so we mix

14:39

we may do cluster and referral sampling

14:42

where we randomly select a geographic

14:45

area that's our cluster right and then

14:48

our respondents can identify others who

14:51

have that same experience and they'll

14:54

refer them to

14:56

us sampling size and Power we'll

14:59

definitely talk more about these things

15:01

but it's important to know that with

15:03

qualitative studies we don't go in with

15:06

a predetermined idea of how many

15:08

subjects we're going to need we're going

15:10

to continue to sample we're going to

15:12

talk to

15:13

people and look at our data begin to

15:18

code our data and determine we start to

15:21

see Trends and

15:23

patterns when we start to see that

15:26

redundancy then we start to look at

15:29

saturation we think we've got all we're

15:31

going to get we've got enough that it's

15:33

not going to

15:35

change

15:37

saturation quantitative samples on the

15:39

other hand we're going to need a certain

15:43

power tell us how powerful our our uh

15:46

data is the greater the number of

15:48

subjects the greater the power the

15:51

greater the significance and and really

15:54

the the magnitude of our results is

15:56

going to be much stronger with

15:59

quantitative samples if we have a large

16:01

sample size and we'll do a Power

16:03

analysis to determine how large it ought

16:06

to be and then we'll try to get that

16:09

number

16:10

of subjects

16:12

right small samples you're concerned

16:15

really that you have a representative

16:17

sample and you can be concerned about

16:21

type two errors and that is that um

16:25

there may be a difference between the

16:27

groups but the groups are so small that

16:30

we can't pick it

16:37

up so when you go to read a subject read

16:40

a study and you're looking at the data

16:43

that's there look at what's being said

16:47

read the study you can't read the title

16:50

or the topic the the title or the

16:53

abstract and really know what it's about

16:55

honestly read the abstract but then read

16:59

more information how were the subjects

17:03

selected was it

17:05

objective was it

17:07

random how was the sampling strategy

17:10

applied was it consistent throughout or

17:13

were there inconsistencies and how they

17:16

ran the

17:17

study how about how they're assigned to

17:19

treatment groups was that random was

17:21

that impartial or did the kind of pick

17:23

and choosey they wanted to be in the

17:25

treatment

17:26

group were there enough subjects

17:29

included that you can feel like the

17:32

results are good and that the

17:33

conclusions

17:35

are um reliable I guess realistic

17:43

true qualitatively you're looking at

17:45

criteria

17:47

established that were the

17:48

characteristics desirable in the

17:50

informance did you establish those did

17:53

you look for those then did the

17:55

informants have those characteristics

18:00

did the researchers apply apply enough

18:02

effort to find respondents who would be

18:05

best for answering informing the

18:08

questions and finally that word

18:10

saturation that you got enough subjects

18:14

and enough information that you weren't

18:17

getting anything new that it wasn't

18:20

changing what you had that you were

18:22

seeing those Trends and themes emerge

18:25

and then you've got saturation

18:30

using research as evidence for practice

18:33

look for threats to validity a lot of

18:38

times we talk about validity and

18:41

reliability validity population validity

18:44

ecological validity is it usable how did

18:48

you define the population what were

18:50

extraneous variables out there maybe you

18:53

caught them maybe you didn't did they

18:56

affect the outcome could they affect

18:58

outcome

19:00

is the setting reasonably similar my

19:03

concern for my study was that because I

19:05

went to clinic and I and I got subjects

19:09

and clinic but then I went to the camp

19:11

setting people checking in the

19:13

camp I hope they were reasonably similar

19:16

my RB decided they were so have they

19:19

been replicated if this is a one study

19:22

and nothing else gets the same findings

19:24

you got to wonder

19:29

so in terms of describing adequate

19:32

sampling strategies Define you've got to

19:35

carefully Define your population you've

19:38

got to have inclusion and exclusion

19:41

criteria who can participate who cannot

19:45

participate that's one way of kind of

19:48

controlling those extraneous variables

19:51

what's your recruitment plan how are you

19:53

going to get subjects to

19:55

participate do your power analysis and

19:58

determine how many subjects you

20:01

need apply the methodology that you

20:04

chose and then do everything you can to

20:07

maximize retention now in my study I did

20:10

a one-time thing and everybody completed

20:13

my questionnaire one time I had three

20:16

questionnaires everybody completed them

20:17

at once so I really didn't have a

20:19

retention issue and I told my subjects

20:23

and their parents that they could

20:25

withdraw from the study at any point up

20:27

until they had completed the

20:30

questionnaires but once they had

20:31

completed my questionnaires they could

20:33

not withdraw after

20:37

that so for chapter seven you're really

20:39

talking about sampling strategies it's

20:42

really

20:43

important uh if we want to apply our

20:46

findings especially to practice right

20:49

it's our way to control

20:51

bias random selection is always best but

20:55

if we can't randomly select from the

20:58

population

20:59

let's randomly select from our group our

21:03

subject

21:05

pool um what else survey designs have

21:08

additional challenges related to

21:09

response rate how many times do you have

21:12

a

21:13

questionnaire and you look at it you

21:15

maybe send it to a thousand people and

21:17

10 people

21:18

responded that's a terrible response

21:21

rate what are you going to do with

21:22

that sample size is important sample

21:25

size tells us how strong it is and we

21:28

want power to be strong it's a concern

21:31

only if there's no statistically

21:34

significant

21:38

results chapter eight talks about

21:40

measurement and data collection kind of

21:42

more of what we're doing measurement is

21:44

a really strong um way to look for and

21:49

to collect good evidence measurement

21:52

makes it possible to make decisions

21:56

right to give us evidence of the

21:59

characteristic we're looking at to

22:00

determine if it's present how present is

22:04

it measurement is based on very

22:06

definitive rules for how we measure and

22:11

it usually involves numbers some way to

22:14

classify or quantify if you will an

22:17

attribute we can do that by instruments

22:20

or classification a lot of instruments

22:23

are out there by instrument it could

22:25

mean a tool which is a survey a lyer

22:29

scale

22:31

survey it could mean a blood pressure

22:33

cuff as an instrument right that's going

22:36

to give us a number was your blood

22:38

pressure higher or lower after the

22:40

treatment let's take your blood pressure

22:43

heart

22:44

ratees things like

22:46

that so we need to Define our variables

22:49

now we can Define the concept of the the

22:54

variable I can Define the concept of

22:57

quality of life such as support and

22:59

self-concept which is what I did what

23:02

does that mean what are the definitions

23:04

really of those Concepts but then

23:08

operationally I Define those as the

23:11

scores the students made on the

23:16

instruments used to represent those

23:21

Concepts so you really need both when

23:24

you're looking at your studies look for

23:25

both

23:29

and I've said before and I'll say again

23:32

make sure you're looking at primary data

23:35

it is really the most common data

23:37

collection method used systematically

23:39

collecting data can be quantitative or

23:43

qualitative data you can do it in person

23:46

by mail you can do it online but you are

23:50

the person collecting the data it's

23:51

primary data whoever is the researcher

23:55

reporting the results they were the data

23:58

collector

23:59

that's primary data they're not reading

24:02

somebody else's work and then

24:04

summarizing it and Reporting on it

24:06

because that one step away from the

24:09

primary

24:10

data could potentially have bias and and

24:13

change it just a little bit so we want

24:16

primary

24:17

data now this is really big to read it's

24:20

in your book and I do want you to go

24:22

back and look at it but survey design

24:25

primary data you can see and secondary

24:27

data

24:29

all of this is here primary data you're

24:31

going to do all of these things

24:33

secondary data it's already done you're

24:35

just looking at somebody else's data

24:37

right primary data what are you going to

24:39

do are you going to do a questionnaire

24:41

are you going to do an

24:43

interview how are you going to do these

24:52

things Clos questions give you options

24:56

but you have to choose an option it's

24:57

close it's

24:59

forced and every option is mutually

25:02

exclusive of every other option in other

25:04

words if I want to know your age I would

25:07

say s

25:09

to8 I couldn't say 8 to 10 because

25:11

Eight's in both right it's not mutually

25:13

exclusive so maybe I would say 7 to 8 9

25:16

to 10 and then I've got mutually

25:20

exclusive and we have our own little

25:22

total range of answers dichotomus you

25:25

have two answers right yes no true false

25:29

it's it's one or the

25:30

other scales are used a lot lyer scales

25:35

especially there are

25:37

continuums of uh where you have a line

25:41

and here's one end and here's the other

25:43

end and then you would mark yourself on

25:46

that line from least to

25:53

most when it comes to survey questions

25:56

and writing survey questions just

25:58

remember they need to be

26:01

short they don't need to be ambiguous

26:04

they should be unambiguous very clear

26:07

they should not be leading they

26:08

shouldn't have emotion attached to them

26:11

okay survey questions now for the most

26:14

part people you wouldn't necessarily

26:17

write your own survey

26:19

questions you're going to choose a

26:21

survey as a researcher hopefully that is

26:25

already out there already been tried and

26:27

true already has validity and

26:29

reliability num so we know it does what

26:32

it's supposed to do right if we write

26:35

our own if we make our own survey then

26:38

we do have to test it for validity and

26:40

reliability before we can actually use

26:42

it in our study but validity and

26:46

reliability of the instruments use

26:48

should always be included in the study

26:51

you'll be asked in your second paper I

26:54

believe about validity and

26:57

reliability so look for that information

27:00

in your

27:03

studies measurement error measurement

27:06

error is the difference between what

27:09

really is true versus what the score

27:13

says is true so we want to know that we

27:16

really are measuring what we're supposed

27:17

to be measuring

27:21

right all right random mirror can be

27:24

affected by a lot of different things

27:25

we'll talk more about that system IC

27:28

area error is just a consistent bias

27:33

it's always in there and maybe this is

27:35

on purpose maybe somebody just doesn't

27:38

know what they're doing but this is why

27:40

we ask you to look at peer-reviewed

27:43

scholarly Journal articles because those

27:46

have been

27:47

reviewed by people who know for these

27:51

kinds of Errors

27:54

so um we want to make sure our equipment

27:56

is calibrated if you're using blood

27:58

pressure cuff we'll have it calibrated

28:00

we'll do blood pressures with it and

28:02

three others do they all get the same

28:04

result then we can be pretty sure that

28:07

it's correct we want to make sure that

28:09

it's consistently measuring the way it's

28:12

supposed

28:16

to reliability tells us how much we can

28:22

reproduce this result we want it to be

28:24

reproducible right we want somebody else

28:27

to take our our information our

28:30

instruments our model and methods and do

28:32

it and get the same results we got

28:36

hopefully if there's stability within

28:38

the instrument that's internal

28:40

reliability each element measures as

28:42

it's supposed to together um you want

28:46

stability in that way you also want

28:49

stability between Raiders if I am going

28:52

to people and asking questions and

28:55

rating their responses then I need to

28:57

know that but this other person going

28:59

and doing the same thing is rating it

29:01

the same way that I am and so if you

29:04

have more than one person doing

29:06

interviews or or rating scales we'll

29:09

have everybody sit down together and

29:11

we'll do them and make sure we all match

29:14

um and then over time you want it to be

29:17

able to over time if we test we retest

29:20

it should still be reliable to measure

29:22

as it's supposed

29:26

to the validity validity does it

29:30

consistently measure

29:33

accurately um it really does reflect the

29:37

content it's supposed to reflect uh test

29:40

blueprints help us determine content

29:44

validity construct validity it does

29:47

represent the concepts that we want to

29:51

know about uh we want concurrent

29:54

predictive discriminate Criterion

29:56

related validity lots of different ways

29:59

to check um and talk about validity but

30:03

the bottom line reliability and validity

30:06

it measures what it's supposed to

30:08

measure and it can do it consistently

30:11

over

30:15

time diagnostic

30:18

measures

30:20

sensitivity of an instrument says that

30:22

it can detect

30:24

disease

30:25

specificity it can detect when the

30:28

disease is not there and responsiveness

30:32

can it test or can it check can it tell

30:36

uh when an intervention is affected does

30:38

it pick up that

30:43

change collecting data using instruments

30:46

a lot of instrumentation is online now

30:50

it's easy right it's low cost I can send

30:52

you a survey monkey and have you do it

30:54

it doesn't cost anything um it's

30:57

accurate

30:59

right it's convenient for the

31:01

participants and for the researcher you

31:04

just can't interact with people

31:05

sometimes I think if you talk to people

31:08

uh maybe they have a better feel for a

31:11

desire to help a desire to want to do it

31:14

but you do have that risk for systematic

31:16

sampling error too in terms of online

31:20

social media you can get a large

31:23

geographic area in a study it is good

31:27

good for hard to- reach

31:29

populations and it's still relatively

31:33

low cost right I saw something on

31:36

Facebook a few days ago a survey that a

31:38

nurse was asking people to

31:40

do um disadvantages privacy right

31:43

ethical concerns potentially because you

31:46

may be seeing information shared by

31:49

others other people may be seeing who

31:51

agrees to

31:53

participate right and then self-

31:56

selection error may be a RIS maybe they

31:57

said oh yeah I'm going to sign up for

31:59

that and they really don't have the

32:02

disease that you're testing for or

32:04

looking

32:05

at Technology based pretty much you get

32:09

higher response rates it's convenient

32:11

for everybody there may be an expense

32:14

though do I have to set up computers or

32:18

tablets um for people to have access to

32:20

to do this I can go to the mall and I

32:23

can have tablets but I have to buy it's

32:25

a lot of equipment

32:28

a lot of variation in the device and how

32:30

they work a lot of them are very user

32:32

friendly and a lot of devices are not

32:35

and it depends a lot on the person an

32:38

older person may have trouble with

32:42

technology interviews are really good

32:44

you can sit down and get a lot of

32:46

information you can talk to the person

32:48

and you can begin like with qualitative

32:50

you begin to hear those

32:53

themes and that information is personal

32:57

but it's time consume me to sit down and

32:58

have an hour an hour conversation with

33:00

somebody when I could give them a

33:02

questionnaire right and that training

33:05

that you need to do an interview we need

33:07

to know we're asking the same questions

33:09

we're looking for the same information

33:12

you're listening for some things that

33:14

that should be there so you do have to

33:17

train to do those

33:21

interviews focus groups um have

33:25

benefits um good information with a

33:27

group group of people they may um not

33:31

want to share with each other U it's

33:34

expensive can be time consuming you need

33:36

a place to meet and all those people you

33:39

probably need some coffee and things

33:41

like that so it also requires a skilled

33:44

facilitator many times have you been in

33:46

the classroom um and seen that it just

33:49

kind of got out of control suddenly and

33:51

so focus groups can do that if

33:53

somebody's needs to be trained to pull

33:56

the group back in and stay on topic it's

33:58

really hard to

34:00

do observation is another one it's not

34:04

invasive um it gives you a lot of good

34:06

information and we talk about all the

34:08

time how much we get from patients just

34:11

observing them and so there you go it

34:15

has disadvantages it can be timec

34:17

consuming depending on how much

34:18

observation is needed and if somebody

34:21

knows you're watching them they may

34:24

change their behavior so there you go

34:27

and you can have direct observation and

34:29

indirect observation versus something

34:32

may be recorded or something like that

34:35

but again I think you've got a little

34:37

bit of change noted if you know you're

34:39

being recorded how does that

34:45

impact uh secondary data that's where

34:49

you have data collected by somebody else

34:52

maybe even for another purpose but now

34:54

you have access to this big huge Data

34:57

Bank and I think I'm going to go pull

34:59

and see how many people in the US were

35:02

admitted for cardiac conditions between

35:05

the ages of 40 and 50 in 2023 you can

35:08

there's a database that you can go and

35:10

pull that information for free um and so

35:13

there that's secondary I didn't go

35:15

collect that data but I know where to

35:18

get it and I went and looked at it's

35:19

very efficient very convenient it

35:22

greatly reduces the time you need to to

35:25

study to go and collect all that data

35:28

yourself right but you do have

35:30

disadvantages in that sometimes the data

35:32

is not complete maybe it's not accurate

35:34

how do you know those blood pressure

35:36

costs were were checked for

35:39

accuracy and you really can't control

35:41

how that data was collected and it is

35:43

retrospective in a bit it's already

35:46

happened and you're looking back on that

35:51

data big data is just that looking at

35:55

vast amounts of data but using data

35:58

science method somehow you can

36:02

do really

36:06

large what's the right word really large

36:09

evaluations of data um but you have low

36:14

error rates it's it's got a high value

36:17

and it's really has a role in

36:20

evidence-based nursing right now we do

36:22

some of those things in terms of

36:23

systematic reviews but this is even on a

36:25

grander scale than that

36:33

if you're doing data collection you do

36:34

need a procedure for data collection you

36:37

would need to write a code book uh

36:39

things as simple as male is one female

36:42

is two and on and on um maybe you would

36:47

code

36:48

ages and so all of that becomes

36:51

important

36:53

right how are you going to manage the

36:55

DAT how are you going to organize data

36:57

how are you going to store the data

36:59

everything has to be locked up I

37:02

panicked I had mine locked in a locked

37:06

box to transport it had a friend who had

37:08

a wreck she had a file box that had a

37:11

wreck and there was her data spelled on

37:13

the highway so you violated

37:16

confidentiality got to be careful mine

37:18

is in a locked box and I still have it

37:21

from 20 years ago by the way because I

37:22

don't know what to do with it I guess I

37:24

should go shred

37:26

it can't share it that individual data

37:30

and we make a point of telling our

37:32

subjects that the data is not going to

37:34

be identified individually but it's

37:37

going to be reported as group data and

37:40

that's what we have to

37:43

do so really measures and data

37:46

collection are a way of doing things

37:48

systematically the more systematic and

37:51

detailed you can be the the higher your

37:55

uh results the greater the quality of

37:58

what you're doing is look for an

38:00

existing instrument remember we talked

38:03

about validity and reliability if you

38:06

make an instrument you've got to

38:07

establish those things first you'll have

38:09

to Pilot it find an instrument that's

38:11

already out there that that's already

38:12

been done on we already know it measures

38:15

what it's supposed to measure we already

38:17

know it does it consistently over time

38:21

so and then be feasible you want to do

38:24

something

38:25

that's you've got the time to do do you

38:28

got the resources to do you've got the

38:30

finances to do you've got the people to

38:33

do it and you've got the time to get it

38:37

done your delivery method needs to be

38:40

consistent with what you want to do in

38:42

your study and your data collection

38:44

protocols have to be

38:48

defined so in this case we looked at

38:50

measurement quantifying

38:53

characteristics lots of different data

38:56

can be Quant Quantified and measured

39:00

measurement error is always present but

39:01

we do everything we can to make it

39:05

minimal instruments have to be valid and

39:08

reliable if you're writing your own

39:10

instrument you've got to establish that

39:12

if you're using one that's already been

39:14

established you've got to report

39:16

validity and reliability you're going to

39:18

be asked to do that in your week five

39:20

project and then you've got to collect

39:22

data systematically and I believe that's

39:25

it for the week isn't it guys

39:28

yay thank you for listening

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