Research Flashcards

1
Q

Cohort Design

A

“Prospective studies” are where a group of identified subjects, exposed to a similar situation are observed over time.
Difference between an RCT and a Cohort study is that the allocation of subjects is not under the control of the investigator because the investigator must find another group of subjects similar to “exposed” in terms of other important factors.
Advantages of Cohort studies are that they are less expensive and less time-consuming than RCT’s.

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2
Q

Single Case Design

A

In this design one subject is followed over time, and evaluated on outcomes of interest. Subject serves as their own “control” and they are evaluated both before and after the intervention. This design is useful when a few clients have a particular diagnosis or are involved in a treatment that you want to evaluate.
Sometime it is difficult to conclude that the treatment alone resulted in any differences as other factors may change over time, for example the disease severity may change.

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3
Q

Before-after design:

A

This design is used to evaluate a group of subjects involved in a treatment where the evaluator collects information about the initial status of a group and compares it with an information about the outcomes after treatment is received.
This is a useful design when you do not wish to withhold treatment from any subjects, however with no “control” group, it is impossible to judge if the treatment alone was responsible for any changes in the outcomes.

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4
Q

Case control design

A

Retrospective study exploring what makes a group of individuals different by looking at an issue after it has happened.
Study compares the differences between subjects with a defining characteristic or situation with a similar (control) group of people who do not have the characteristic or are not involved in the situation of interest.
Design is inexpensive with problems related to difficulties to conclude what factors are responsible for the outcomes.

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5
Q

Cross Sectional Design

A

By using surveys, questionnaires and interviews this design is used to explore factors that may have influenced a particular outcome in a group of people. Evaluation of the group is carried out at the same time and it is useful when little is known about an issue.
Limitation is that it is impossible to know if all factors have been evaluated, so it is difficult to draw cause-effect conclusions from the results beyond the group of people being studied.

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6
Q

Case Study Design

A

A case study is carried out in order to provide descriptive information about the relationship between a particular treatment and an outcome of interest. There is no control group.
It is often used to explore a new treatment, when there is little knowledge but the results can only be considered in terms of describing a particular situation.
It may generate information to support further study of the topic of interest

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7
Q

Biases

A

A bias affects the results of a study either by favoring the treatment group or the control group.
The most common biases are:
1. Sample selection biases - subjects in the sample being unrepresentative of the population which you are interested in
2. Measurement biases - related to how the outcome of interest was measured
3. Intervention biases- involves how the treatment itself was carried out.

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8
Q

Sample selection biases

A

subjects in the sample being unrepresentative of the population which you are interested in

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9
Q

Measurement biases

A

related to how the outcome of interest was measured

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10
Q

Intervention biases

A

involves how the treatment itself was carried out.

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11
Q

Volunteer or referral bias

A

People who volunteer to participate in a study, or who are referred to a study by someone are often different than non-volunteers/non-referrals. This bias usually, but not always, favors the treatment group, as volunteers tend to be more motivated and concerned about their health.

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12
Q

Seasonal bias

A

If all subjects are recruited and thus are evaluated and receive treatment at one time, the
results may be influenced by the timing of the subject selection and intervention. For
example, seniors tend to be healthier in the summer than the winter, so the results may be
more positive if the study takes place only in the summer. This bias could work in either direction, depending on the time of year`

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13
Q

Attention bias

A

People who are evaluated as part of a study are usually aware of the purpose of the study, and as a result of the attention, give more favorable responses or perform better than people who are unaware of the study’s intent. This bias is why some studies use an “attention control” group, where the people in the control group receive the same amount of attention as those people in the treatment group, although it is not the same treatment.

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14
Q

Measurement Biases

A

Number of outcome measures used:
Bias can be introduced if only one outcome measure is used or if there are too many outcome measures for the sample size
Lack of “masked” or “independent” evaluation:
If the evaluators are aware of which group a subject was allocated to, or which treatment a person received, it is possible for the evaluator to influence the results by giving the person or group of people, a more or less favorable evaluation. It is usually the treatment group that is favored.

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15
Q

Recall or memory bias:

A

This can be a problem if outcomes are measured using self-report tools, surveys or interviews that are requiring the person to recall past events. Often a person recalls positive memories more than negative ones, and this can favor the results of the study for those people being questioned about an issue or receiving treatment.

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16
Q

Contamination

A

This occurs when members of the control group inadvertently receive treatment, thus the difference in outcomes between the two groups may be reduced. This favors the control group.

17
Q

co-ontervention

A

If subjects receive another form of treatment at the same time as the study treatment, this can influence the results in either direction.

18
Q

Timing of intervention

A

Different issues related to the timing of intervention can introduce a bias. If treatment is provided over an extended period of time to children, maturation alone could be a factor in improvements seen.

19
Q

Site of treatment:

A

Where treatment takes place can influence the results and should be consistent among all groups.

20
Q

Different therapists:

A

If different investigators are involved in providing the treatments to the different groups of subjects the results could be influenced in different directions.
Investigator involvement should be equal and consistent between all treatment groups

21
Q

N = ?

A

The number of subjects/clients involved in the study should be clear.
The description of the sample should be detailed enough for you to have a clear picture of who was involved.
Important characteristics related to the topic of interest should be reported, in order to conclude that the study population is similar to your own and that bias was minimized.
The authors should state how they arrived at the sample size, to justify why the number was chosen. Often, justification is based on the population available for study. Some authors provide statistical justification for the sample size, but this is rare.
Ethics procedures should be described, although they are often left out. At the very least, authors should report if informed consent was obtained at the beginning of the study.

22
Q

sample: Important characteristics include:

A
  • Who makes up the sample; are the subjects appropriate for the study question and described in terms of age, gender and functional status?
    • How many subjects were involved, and if there are different groups that are relatively equal in size?
    • How the sampling was done; was it voluntary or by referral and were inclusion and exclusion criteria described?
23
Q

DEVELOP DESIGN THAT HAS CONSTRUCT INTERNAL AND EXTERNAL VALIDITY

A

well developed constructs and well developed independent and dependent variables
manipulation, control, randomization
design to minimize confounding factors while being feasible and practical
generalizability of research

24
Q

external validity

A

A study that readily allows its findings to generalize to the population at large

25
Q

internal validity.

A

To the degree that we are successful in eliminating confounding variables within the study itself

26
Q

EVALUATE RESEARCH FOR INTERNAL, EXTERNAL AND CONSTRUCT VALIDITY

A

what were the levels of manipulation, control, and randomization
what are confounding factors in the study
what needs modification in lights of results:
theory
constructs
design
variables as defined and measured
other
how genearlizable are the results of the study

27
Q

DEVELOP VALID AND RELIABLE MESUREMENT OF THE INDEPENDENT AND DEPENDENT VARIABLES

A

units of measure discrete, continuous, ability to generalize
levels of independent variables
measurement of the dependent variables

28
Q

Independent variables

A

An independent variable is the variable you have control over, what you can choose and manipulate. It is usually what you think will affect the dependent variable. In some cases, you may not be able to manipulate the independent variable. It may be something that is already there and is fixed, something you would like to evaluate with respect to how it affects something else, the dependent variable like color, kind, time.

29
Q

Dependent variables

A

A dependent variable is what you measure in the experiment and what is affected during the experiment. The dependent variable responds to the independent variable. It is called dependent because it “depends” on the independent variable. In a scientific experiment, you cannot have a dependent variable without an independent variable.

30
Q

Multiple Variables

A

There may be more than one dependent variable and/or independent variable. This is especially true if you are conducting an experiment with multiple stages or sets of procedures. In these experiments, there may be more than one set of measurements with different variables

31
Q

RECORD & EVALUATE MEASUREMENTS

A

check measure for accuracy
compute statistic and evaluate data
check assumptions for valid test statistic and modify if necessary

32
Q

SELECT TEST STATISTIC

A

appropriate to hypothesis and research design
consider assumptions for valid test statistic
determine meaningful difference, both clinical and statistical
determine acceptable level of power/error
determine size sample that is necessary based on test statistic, direction of the hypothesis and level of power/error

33
Q

Interpret results, discussions and conclusions:

A

meaning and utility of study
alternative explanations for the results
applicability to current practice
implication for future research

34
Q

RESEARCH PROCESS

A

WRITE AND SUBMITT ON TIME RESEARCH PROPOSAL
WRITE INFROMED CONSENT
WRITE AND SUBMIT ON TIME NECESSARY IRB FORMS
RANDOMLY SAMPLE AND RANDOMLY ASSIGN UNITS OR SUBJECTS TO TREATMENT
IMPLEMENT STUDY AS DESIGNED
Prepare materials for professional communication
paper for faculty review
poster
platform presentation
publication

35
Q

INFORMED CONSENT

A

Disclosure:
the nature of the condition
the long-term effect of the condition
the effect of non treating the condition
the nature of available treatments
anticipated benefits of proposed procedures
the probability of achieving these benefits
potential risk of undergoing the procedure
Comprehension
describe procedures in lay language
visually appealing written material
provide ample time for explaining procedure
allow ample time before requiring a decision
Voluntariness
Competence - legality and guardianship