• Wrong document? Swap it for free
  • Written by students who passed
  • Immediately available after payment
  • Read online or as PDF
Sell
Where do you study
Your language
Document preview thumbnail
Preview 4 out of 71 pages
Exam (elaborations)

PSYC 255 Comprehensive Final Exam – Introduction to Research |Questions and Answers | 2026/27 Update | A+ Guide | 100% Correct - LU.

Document preview thumbnail
Preview 4 out of 71 pages

PSYC 255 Comprehensive Final Exam – Introduction to Research |Questions and Answers | 2026/27 Update | A+ Guide | 100% Correct - LU.

Content preview

PSYC 255 Comprehensive Final Exam - Introduction to Research
| Questions and Answers | 2026/27 Update | 100% Correct - LU. -
Questions and Answers Already Graded A+ Premium Exam
Tested And Verified


Subject Area Psychology - Research Methods and Statistics

Description This comprehensive final exam assesses mastery of research methodology,
quantitative and qualitative designs, psychometrics, statistical inference, and
research ethics as taught in PSYC 255 at Liberty University. It emphasizes
application of APA-style empirical reasoning and a biblically-informed,
ethically-grounded approach to psychological science.

Expected Grade A+

Total Questions 150

Duration 3 hours

Learning Outcomes 1. Differentiate experimental, quasi-experimental, correlational, and qualitative
research designs and select the design best suited to a given research question.
2. Interpret reliability, validity, effect size, and statistical significance evidence to
evaluate psychological measures and study claims.
3. Apply ethical principles and Liberty University's Christian worldview
commitments to the design, conduct, and reporting of psychological research.

Accreditation Aligned with US regional accreditation standards (SACSCOC) and APA
undergraduate psychology guidelines for research methods coursework.




Page 1

,1. A researcher wants to test whether a new gratitude journaling intervention
causes improved life satisfaction. Which design provides the strongest causal
evidence?
A. A cross-sectional survey correlating journaling frequency with satisfaction scores.
B. A randomized controlled trial assigning participants to journaling or waitlist
conditions.
C. A longitudinal study tracking volunteers who chose to journal for six months.
D. A qualitative interview study exploring participants' journaling experiences.
Answer: B. A randomized controlled trial assigning participants to
journaling or waitlist conditions.

Random assignment in an RCT controls for confounding variables and allows
causal inference, which is the hallmark of true experiments. Correlational and
self-selected designs (A, C) cannot rule out third-variable explanations, and
qualitative designs (D) describe rather than establish causation.

2. A scale yields Cronbach's alpha = .62. What is the most appropriate
psychometric interpretation?
A. The scale has excellent internal consistency and is ready for clinical use.
B. The scale has acceptable test-retest reliability but poor internal consistency.
C. The scale's internal consistency is below the commonly accepted threshold of .70.
D. The scale demonstrates strong convergent validity with related measures.
Answer: C. The scale's internal consistency is below the commonly accepted
threshold of .70.

Cronbach's alpha estimates internal consistency; values below .70 are generally
considered inadequate for research purposes. Alpha does not directly assess
test-retest reliability (B) or validity (D), and .62 is not excellent (A).




Page 2

,3. Which sampling method most threatens external validity by relying on
volunteers who self-select into a study?
A. Stratified random sampling
B. Cluster sampling
C. Convenience sampling
D. Systematic sampling
Answer: C. Convenience sampling

Convenience sampling uses readily available, self-selected participants, which
limits generalizability to the broader population. Stratified, cluster, and
systematic sampling are probability-based methods that better support external
validity.

4. A researcher reports a p-value of .03. Which interpretation is correct under
null hypothesis significance testing?
A. There is a 3% probability that the null hypothesis is true.
B. There is a 3% probability of obtaining results at least as extreme if the null
hypothesis were true.
C. The effect size is large and practically significant.
D. The results are clinically meaningful and should change practice.
Answer: B. There is a 3% probability of obtaining results at least as extreme
if the null hypothesis were true.

A p-value indicates the probability of observing data at least as extreme as
obtained, assuming the null hypothesis is true. It does not give the probability of
the null being true (A), nor does it measure effect size or practical significance (C,
D).




Page 3

, 5. Which research design is most vulnerable to the placebo effect and demand
characteristics?
A. Double-blind randomized controlled trial
B. Single-blind randomized controlled trial
C. Open-label randomized controlled trial
D. Waitlist controlled trial with blinded assessors
Answer: C. Open-label randomized controlled trial

Open-label trials do not blind participants or researchers, maximizing placebo
effects and demand characteristics. Double-blind, single-blind, and
blinded-assessor designs reduce these biases.

6. A researcher wants to describe the lived experience of forgiveness among
cancer survivors. Which approach is most appropriate?
A. A factorial ANOVA comparing forgiveness scores across groups.
B. A phenomenological qualitative study using in-depth interviews.
C. A correlational study linking forgiveness to cortisol levels.
D. A meta-analysis of forgiveness interventions.
Answer: B. A phenomenological qualitative study using in-depth interviews.

Phenomenology is designed to capture the essence of lived experiences through
rich, subjective accounts. ANOVA, correlational, and meta-analytic designs test
relationships or aggregate effects rather than explore personal meaning.

7. Which statement best reflects the ethical principle of beneficence in
research?
A. Participants must be fully informed and voluntarily consent.
B. Researchers must maximize benefits and minimize harms.
C. Participant data must be kept confidential.
D. Vulnerable populations must be excluded from all studies.
Answer: B. Researchers must maximize benefits and minimize harms.

Beneficence requires balancing potential benefits against risks and minimizing
harm. Informed consent reflects autonomy (A), confidentiality reflects privacy
(C), and excluding vulnerable groups is not a requirement of beneficence (D).




Page 4

Document information

Uploaded on
September 24, 2026
Number of pages
71
Written in
2026/2027
Type
Exam (elaborations)
Contains
Questions & answers
$25.49

Wrong document? Swap it for free Within 14 days of purchase and before downloading, you can choose a different document. You can simply spend the amount again.
Written by students who passed
Immediately available after payment
Read online or as PDF

Seller avatar
Reputation scores are based on the amount of documents a seller has sold for a fee and the reviews they have received for those documents. There are three levels: Bronze, Silver and Gold. The better the reputation, the more your can rely on the quality of the sellers work.
ProfReginaBank
4.7
(3)
Sold
20
Followers
2
Items
1543
Last sold
5 days ago



Why students choose Stuvia

Created by fellow students, verified by reviews

Quality you can trust: written by students who passed their tests and reviewed by others who've used these notes.

Didn't get what you expected? Choose another document

No worries! You can instantly pick a different document that better fits what you're looking for.

Pay as you like, start learning right away

No subscription, no commitments. Pay the way you're used to via credit card and download your PDF document instantly.

Student with book image

“Bought, downloaded, and aced it. It really can be that simple.”

Alisha Student

Working on your references?

Create accurate citations in APA, MLA and Harvard with our free citation generator.

Working on your references?

Frequently asked questions