- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06341569
Physical Therapy Students: Well-being
Understanding Well-being in Physical Therapy Students: A Multi-Dimensional Analysis of Motivation, Life Satisfaction, and Perceived Academic Quality
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Understanding the psychosocial state of academic students has become a primary concern in contemporary educational research and practice. As students go through the challenges of higher education, factors such as motivation, life satisfaction, and happiness play crucial roles in shaping their academic experiences and outcomes. Therefore, researchers have increasingly turned their attention to studying these elements in order to gain insight into the overall state of students and inform strategies designed to create positive educational outcomes.
The implications of studying motivation, life satisfaction, and happiness among academic students are far-reaching. By gaining a deeper understanding of these psychosocial elements, educators and policymakers can develop interventions and programs designed to cultivate positive learning environments that support students' psychological well-being and academic success. For example, strategies that enhance intrinsic motivation, such as promoting autonomy and providing meaningful learning opportunities, can lead to improved engagement and academic achievement. Similarly, initiatives that promote a sense of belonging and social support can improve students' overall life satisfaction and happiness.
Thus, this study aims to explore various psychosocial aspects and the potential benefits of respiratory techniques for physical therapy students.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Timiș County
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Timișoara, Timiș County, Romania, 3003001
- University of Medicine and Pharmacy Victor Babes Timisoara
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Students: enrolled in the physical therapy study program (year I, II and III) Age: > 18 years Ability to understand and follow instructions Availability to provide informed consent.
Exclusion Criteria:
Pre-existing medical conditions: uncontrolled medical conditions (cardiovascular disease, severe respiratory problems) Use of psychotropic drugs: drugs that could significantly affect mood, anxiety level, or sleep quality.
Pregnancy: due to potential physiological changes that could influence the results of the study.
Inability to comply with study requirements: these could include completing questionnaires and participating in the respiratory techniques program (if part of the intervention group).
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: Non-Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Respiratory breathing techniques group
Subjects included in the intervention group will receive a 14 week breathing technique program that will include: different types of breathing techniques (diaphragmatic, pursed-lips, alternate nostril breathing, etc.); progressive muscle relaxation techniques; and medical education about breathing.
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Target group: subjects in the respiratory breathing techniques group. Program duration: the program lasts for 14 weeks. Breathing techniques: the program includes various breathing exercises, including: Diaphragmatic breathing teaches participants to breathe deeply, engaging the diaphragm muscle, which can improve lung capacity and relaxation. Pursed-lips breathing: this technique involves inhaling through the nose and exhaling slowly through pursed lips, which can help slow down breathing and manage shortness of breath. Alternate nostril breathing: this technique involves closing one nostril while inhaling and exhaling through the other nostril alternately. Relaxation techniques: the program incorporates progressive muscle relaxation techniques. This involves progressively tensing and relaxing different muscle groups. Medical education: topics like the anatomy of the respiratory system, the importance of proper breathing, potential benefits of specific breathing exercises. |
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No Intervention: Control group
Second-year physical therapy students that do not want to participate in the breathing technique program and will complete only the questionnaires.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Assessing intrinsic and extrinsic motivation levels among physical therapy students.
Time Frame: At the beginning of the study
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The Motivational Styles Questionnaire (MSLQ) assesses students' intrinsic and extrinsic motivation levels.
The MSLQ does not have a standard range of minimum and maximum values.
Higher scores on intrinsic motivation indicate a better outcome, reflecting a higher level of internal motivation.
Conversely, higher scores on extrinsic motivation may suggest a reliance on external rewards or pressures, which could indicate a less favorable outcome.
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At the beginning of the study
|
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Assessing the happiness levels of the students participating in the study.
Time Frame: At the beginning of the study
|
The Oxford Happiness Questionnaire evaluates happiness levels.
It ranges from 1 to 6. Higher scores on the Oxford Happiness Questionnaire indicate a better outcome, reflecting higher happiness and life satisfaction levels.
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At the beginning of the study
|
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Assessing the positive and negative emotional states of the students participating in the study.
Time Frame: At the beginning of the study
|
The PANAS-GEN Questionnaire measures positive and negative expressions to provide insights into emotional states.
It ranges from 1 to 5. Higher scores on positive expressions indicate a better outcome, reflecting higher positive emotions.
Conversely, higher scores on negative expressions may suggest a less favorable outcome, indicating higher levels of negative emotions.
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At the beginning of the study
|
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Assessing the well-being of the students participating in the study.
Time Frame: At the beginning of the study
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The RYFF Psychological Well-being Questionnaire assesses different aspects of psychological well-being among students.
The RYFF Psychological Well-being Questionnaire typically ranges from 1 to 6. Higher scores on the RYFF Psychological Well-being Questionnaire indicate a better outcome, reflecting higher levels of psychological well-being.
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At the beginning of the study
|
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Assessing the overall life satisfaction levels of the students participating in the study.
Time Frame: At the beginning of the study
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The Satisfaction with Life Questionnaire evaluates overall life satisfaction.
It ranges from 1 to 7. Higher scores on the Satisfaction with Life Questionnaire indicate a better outcome and reflect higher levels of life satisfaction.
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At the beginning of the study
|
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Assessing the subjective happiness levels of the students participating in the study.
Time Frame: At the beginning of the study
|
The Subjective Happiness Scale assesses subjective happiness levels.
It ranges from 1 to 7. Higher scores on the Subjective Happiness Scale indicate a better outcome, reflecting higher levels of subjective happiness.
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At the beginning of the study
|
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Assessing the sleep quality of the students participating in the study.
Time Frame: At the beginning of the study
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The Pittsburgh Quality of Sleep Index (PSQI) evaluates the sleep quality of the participants.
It ranges from 0 to 21. Lower scores on the PSQI indicate a better outcome, reflecting higher sleep quality.
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At the beginning of the study
|
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Assessing the worry and anxiety levels of the students participating in the study.
Time Frame: At the beginning of the study
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The Penn State Worry Questionnaire (PSWQ) assesses students' worry and anxiety levels.
It ranges from 1 to 5. Lower scores on the PSWQ indicate a better outcome, reflecting lower levels of worry and anxiety.
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At the beginning of the study
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Assessing the effects of the respiratory techniques program on the intrinsic and extrinsic motivation levels of the students participating in the study.
Time Frame: 14 weeks after the beginning of the study
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Comparison of the MSLQ baseline scores before and after 14 weeks of the respiratory techniques program.
Higher scores on intrinsic motivation indicate a better outcome, reflecting a higher level of internal motivation.
Conversely, higher scores on extrinsic motivation may suggest a reliance on external rewards or pressures, which could indicate a less favorable outcome.
|
14 weeks after the beginning of the study
|
|
Assessing the effects of the respiratory techniques program on the happiness levels of the students participating in the study.
Time Frame: 14 weeks after the beginning of the study
|
Comparison of the Oxford Happiness Questionnaire baseline scores before and after 14 weeks of the respiratory techniques program.
Higher scores on the Oxford Happiness Questionnaire indicate a better outcome, reflecting higher happiness and life satisfaction levels.
|
14 weeks after the beginning of the study
|
|
Assessing the effects of the respiratory techniques program on the students' positive and negative emotional states.
Time Frame: 14 weeks after the beginning of the study
|
Comparison of the PANAS-GEN Questionnaire baseline scores before and after 14 weeks of the respiratory techniques program.
Higher scores on positive expressions indicate a better outcome, reflecting higher positive emotions.
Conversely, higher scores on negative expressions may suggest a less favorable outcome, indicating higher levels of negative emotions.
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14 weeks after the beginning of the study
|
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Assessing the effects of the respiratory techniques program on the students' well-being.
Time Frame: 14 weeks after the beginning of the study
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Comparison of the RYFF Psychological Well-being Questionnaire baseline scores before and after 14 weeks of the respiratory techniques program.
Higher scores on the RYFF Psychological Well-being Questionnaire indicate a better outcome, reflecting higher levels of psychological well-being.
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14 weeks after the beginning of the study
|
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Assessing the effects of the respiratory techniques program on the overall life satisfaction levels of the students participating in the study.
Time Frame: 14 weeks after the beginning of the study
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Comparison of the Satisfaction with Life Questionnaire baseline scores before and after 14 weeks of the respiratory techniques program.
Higher scores on the Satisfaction with Life Questionnaire indicate a better outcome, reflecting higher levels of life satisfaction.
|
14 weeks after the beginning of the study
|
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Assessing the effects of the respiratory techniques program on the subjective happiness levels of the students participating in the study.
Time Frame: 14 weeks after the beginning of the study
|
Comparison of the Subjective Happiness Scale baseline scores before and after 14 weeks of the respiratory techniques program.
Higher scores on the Subjective Happiness Scale indicate a better outcome, reflecting higher levels of subjective happiness.
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14 weeks after the beginning of the study
|
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Assessing the effects of the respiratory techniques program on the quality of sleep of the students participating in the study.
Time Frame: 14 weeks after the beginning of the study
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Comparison of the Pittsburgh Quality of Sleep Index (PSQI) baseline scores before and after 14 weeks of the respiratory techniques program.
Lower scores on the PSQI indicate a better outcome, reflecting higher sleep quality.
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14 weeks after the beginning of the study
|
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Assessing the effects of the respiratory techniques program on the worry and anxiety levels of the students participating in the study.
Time Frame: 14 weeks after the beginning of the study
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Comparison of the Penn State Worry Questionnaire (PSWQ) baseline scores before and after 14 weeks of the respiratory techniques program.
Lower scores on the PSWQ indicate a better outcome, reflecting lower levels of worry and anxiety
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14 weeks after the beginning of the study
|
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Adherence to breathing exercises at 12-month follow-up
Time Frame: 12 months after the end of the intervention
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Adherence will be assessed using a structured self-report questionnaire developed for this study.
Key variables include: weekly frequency, session duration, technique used, barriers, and perceived utility.
A composite dose index (frequency × duration) and binary adherence variable will be calculated.
Full questionnaire, codebook, and scoring instructions are available at: https://doi.org/10.17605/OSF.IO/T9XAP
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12 months after the end of the intervention
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Coping strategies assessed with the COPE at 12-month follow-up
Time Frame: 12 months after the end of the intervention
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Coping will be measured using the COPE inventory (50-item version).
The scale includes multiple subscales such as active coping, emotional support, denial, acceptance, planning, and others.
Subscale scores will be computed according to the scoring manual.
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12 months after the end of the intervention
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Self-esteem assessed with the Rosenberg Self-Esteem Scale at 12-month follow-up
Time Frame: 12 months after the end of the intervention
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Self-esteem will be measured using the Rosenberg Self-Esteem Scale (RSES), a 10-item validated questionnaire.
Higher total scores indicate higher self-esteem.
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12 months after the end of the intervention
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Perceived psychological benefit of breathing practice at 12-month follow-up
Time Frame: 12 months after the end of the intervention
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Psychological benefit will be evaluated using four Likert-scale items measuring perceived improvement in stress, sleep, positivity, and worry.
A composite mean score will be calculated (Perceived_benefit_mean).
Instrument details and scoring instructions are available at: https://doi.org/10.17605/OSF.IO/T9XAP
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12 months after the end of the intervention
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Collaborators and Investigators
Investigators
- Principal Investigator: Alexandru Florian Crisan, PhD, University of Medicine and Pharmacy "Victor Babes" Timisoara
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 11/07.03.2024
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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