- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07244224
The Effect of a Psychosocial Adjustment Program on Healthy Lifestyle Behaviors and Sleep Deprivation in Ninth-Grade Boarding Female Students
The Effect of a Psychosocial Adjustment Program on Healthy Lifestyle Behaviors and Sleep Deprivation in Ninth-Grade Boarding Female Students:A Non-Randomized Controlled Study
The World Health Organization defines adolescence as the ages between 10 and 19, emphasizing that supporting both the mental and physical health of this age group is crucial for determining the individual's future quality of life. Problems such as stress, anxiety, depression, maladjustment, substance use, and sleep disorders faced by adolescents can negatively affect the development of healthy lifestyle behaviors.
In this context, students living in boarding school settings represent a more vulnerable group in terms of the need for psychosocial support, as they live away from their families. Boarding students experience difficulties in adaptation due to homesickness, lack of social support, academic pressures, and a strictly regulated lifestyle, and this situation directly affects their health behaviors.
In this study, the effectiveness of a psychosocial adjustment program will be evaluated with intervention and control groups formed on a voluntary basis from ninth-grade female boarding students studying at two public boarding science high schools located in Antalya, Türkiye. The intervention group will participate in a psychosocial adjustment program developed by the researcher, consisting of five sessions, while the control group will not receive any intervention. The program includes structured and interactive group activities on themes such as adopting healthy lifestyle habits, stress and anxiety management, social support, sleep hygiene, effective communication, academic adjustment, and emotional relaxation.
The data will be collected in three phases as pre-test, post-test, and follow-up test; the data collection tools will include the Personal Information Form, the Health-Promoting Lifestyle Profile II (HPLP II), and the Sleep Deprivation Scale for Children and Adolescents. The data will be analyzed using the SPSS program, and depending on normal distribution, parametric or non-parametric tests will be applied. The effect of the intervention will be measured with Cohen's d to calculate the effect size. This study holds original value as it develops a school-based intervention model under the leadership of a school health nurse, and it may provide an innovative contribution based on a holistic nursing approach to adolescents by taking its place among the limited psychosocial intervention studies conducted in boarding school settings.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Antalya, Turkey (Türkiye)
- Akdeniz Universitesi
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Psychosocial Adaptation Program
In the study, while the intervention group will participate in a five-day psychosocial adjustment program, no intervention will be conducted in the control group.
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It is a five-day psychosocial adjustment program designed for female boarding high school students.
It focuses on promoting healthy lifestyle and improving sleep comfort.
The program includes group education sessions and activity-based interventions tailored to this age group.
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No Intervention: Control group
No intervention will be administered to the control group.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Healthy Lifestyle Behaviors Scale II
Time Frame: Baseline, 4 weeks after baseline, 17 weeks after baseline
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Healthy Lifestyle Behaviors Scale II: The Healthy Lifestyle Behaviors Scale II is used to evaluate individuals' healthy lifestyle behaviors.
The scale consists of a total of 52 items and includes six subscales: spiritual growth, health responsibility, physical activity, nutrition, interpersonal relations, and stress management.
The overall score of the scale indicates the level of healthy lifestyle behaviors.
As the total score increases, it is interpreted that the individual has more healthy lifestyle behaviors.
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Baseline, 4 weeks after baseline, 17 weeks after baseline
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Sleep Deprivation Scale for Children and Adolescents
Time Frame: Time Frame: Baseline, 4 weeks after baseline, 17 weeks after baseline
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Sleep Deprivation Scale for Children and Adolescents: This scale is used to assess sleep deprivation in participants.
Measurements will be taken before and after the intervention.
The scale consists of 15 items rated on a Likert-type scale ranging from "strongly agree" to "strongly disagree."
Scores on the scale range from 15 to 60. Higher scores indicate worse sleep deprivation.
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Time Frame: Baseline, 4 weeks after baseline, 17 weeks after baseline
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: Habibe ARSLAN, Bağlantısız
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 (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- TBAEK-714
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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