Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT06101953 |
Other study ID # |
HU23INSPIRE |
Secondary ID |
E-68552689-000-0 |
Status |
Completed |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
February 27, 2023 |
Est. completion date |
June 11, 2023 |
Study information
Verified date |
October 2023 |
Source |
Hacettepe University |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
The goal of this observational study is to explore the impact of a 12-week online
knowledge-sharing program focusing on stress management, psychological resilience, and
interoception in university students who face various stressors. The primary questions it
aims to answer are:
- How does participating in the online program influence students' understanding and
management of stress?
- Can engaging in this program enhance students' resilience in the face of academic and
life challenges?
- Does the program improve students' interoception skills, helping them recognize and
manage internal bodily sensations and emotions more effectively?
Participants will be asked to:
- Attend weekly sessions covering topics such as stress, its sources, stages, diseases
related to stress, coping methods, psychological resilience, and interoception.
- Engage in discussions, self-reflection, and practical exercises.
- Share their experiences and insights.
- Complete assessments to measure their perceived stress level, resilience, and
interoceptive awareness.
Researchers will compare the group that participates in the program with a control group to
determine if the program significantly improves stress management, enhances psychological
resilience, and bolsters interoception skills among university students.
Description:
Participants and Sampling: The study sample consisted of university students enrolled in the
Department of Occupational Therapy at Hacettepe University Faculty of Health Sciences,
particularly those taking the Stress Coping Methods course. The determination of the sample
size was guided by a rigorous statistical approach, employing G Power for power analysis.
Following this, randomization was performed to create both a control group and an
intervention group. The inclusion criteria required participants to be at least 18 years old,
studying at a university in Turkey, and having Turkish as their native language. The sole
exclusion criterion was the presence of any psychiatric diagnosis, ensuring the homogeneity
of the sample.
Study Procedure: The intervention program, stretching over 12 weeks, was based on the Stress
Coping Mechanisms lecture, derived from various resources such as Pendleton and Schultz-Khron
(2001), Brown et al. (2019), and Reitz et al. (2020). Delivered by a seasoned practitioner
with over 20 years of expertise in stress coping education, the program consisted of three
hours per week. The curriculum was thoughtfully structured to ensure a comprehensive
understanding of stress, its sources, stages, diseases associated with stress, coping
strategies, psychological resilience, and interoception.
The online knowledge-sharing format encouraged interactivity, with participants engaging in
discussions, self-reflection, and practical exercises. As part of the learning process,
students were encouraged to conduct self-inquiries and present their findings to the class.
The program aimed to provide students with a profound understanding of stress, emphasizing
the critical role of psychological resilience and interoception in effective stress
management and overall well-being.
Statistical Analysis: The statistical analysis was carried out using SPSS v26 software. The
Kolmogorov-Smirnov test was used to assess the normality of all variables. Descriptive
statistics were applied, including frequency, percentage, mean, minimum, maximum, and
standard deviation for categorical and numerical variables. To evaluate differences between
categorical variables, the chi-square test was employed. The Wilcoxon signed-rank test was
used to compare baseline and final scores, while the Mann-Whitney U test compared the results
between the control and intervention groups. The significance level was set at p<0.05.
Detailed statistical analyses were guided by a predefined analytical plan that encompassed
both primary and secondary objectives as outlined in the study protocol. Quality assurance,
data validation, and other registry-specific procedures were followed in line with best
practices, ensuring data integrity and the accuracy of the results. Site monitoring and
auditing, data checks for data quality, and source data verification were integral parts of
the quality assurance plan. Additionally, a data dictionary containing detailed variable
descriptions, as well as Standard Operating Procedures for various registry operations, was
meticulously maintained. Further components included sample size assessment, a plan for
addressing missing data, and a comprehensive statistical analysis plan to address the primary
and secondary objectives as specified in the study protocol.