Effects of a Nurse-Led Self-Compassion and Kindness Program on Compassion and Healthy Peer Relationships in Adolescents
Condition(s) studied
Investigational drug(s) / intervention(s)
Nurse-Led Self-Compassion and Kindness Program: This is a 6-week, 40-minute program implemented once a week, focusing on developing compassion and kindness towards themselves and their peers. The program aims to strengthen adolescents' compassion for themselves and others, thereby improving their peer relationships.
Study summary
The goal of this experimental study is to learn if the Nurse-Led Self-Compassion and Kindness Program works to improve self-compassion, compassion toward peers, and peer relationships among adolescents. The main hypotheses to be tested in the study are:
Post-intervention self-compassion scale scores will be significantly higher in the experimental group compared to the control group.
Post-intervention compassion scale scores will be significantly higher in the experimental group compared to the control group.
Post-intervention peer relationships scale scores will be significantly higher in the experimental group compared to the control group.
Follow-up self-compassion scale scores will be significantly higher in the experimental group compared to the control group.
Follow-up compassion scale scores will be significantly higher in the experimental group compared to the control group.
Follow-up peer relationships scale scores will be significantly higher in the experimental group compared to the control group.
Researchers will compare the experimental group (receiving the program) to a control group to see if the Nurse-Led Self-Compassion and Kindness Program is effective in enhancing compassion and peer relationships in adolescents.
Participants will:
Participate in the Nurse-Led Self-Compassion and Kindness Program 1 day a week for 6 weeks
Complete the pre-test, post-test, and follow-up test questionnaires
Eligibility
Primary outcome measure(s)
- Self-Compassion Scale (SCS-SF)-Change in Self-Compassion Levels From Baseline to Post-Intervention (Week 6) — Baseline and immediately after the 6-week intervention
This outcome measure evaluates the immediate effect of the 6-week intervention program on adolescents' self-compassion levels. Self-compassion will be assessed using the Self-Compassion Scale. The scale is a single-dimensional, 5-point Likert-type instrument consisting of 11 items, with responses ranging from 1 ('Never') to 5 ('Always'). The minimum and maximum achievable scores on the scale are 11 and 55, respectively. Higher scores indicate higher levels of self-compassion. - Compassion Scale for Adolescents (CSA) - Change in Compassion Levels From Baseline to Post-Intervention (Week 6) — Baseline and immediately after the 6-week intervention
This outcome measure evaluates the immediate effect of the 6-week intervention program on compassion levels among adolescents. Compassion will be measured using the Compassion Scale for Adolescents. The Compassion Scale for Adolescents (CSA) is a 5-point Likert-type instrument consisting of 30 items across six subscales, with responses ranging from 1 ('Strongly disagree') to 5 ('Strongly agree'). The total achievable score on the scale ranges from a minimum of 30 to a maximum of 150. Higher total scores indicate higher levels of compassion. - Peer Relationships Scale (PRS) - Change in Peer Relationships From Baseline to Post-Intervention (Week 6) — Baseline and immediately after the 6-week intervention
This outcome measure evaluates the improvement in peer relationships following the 6-week intervention program. Peer relationships will be assessed using the Peer Relationships Scale. The Peer Relationships Scale (PRS) is a 5-point Likert-type instrument consisting of 29 items across four subscales, with responses ranging from 1 ('Strongly disagree') to 5 ('Strongly agree'). The minimum and maximum achievable total scores on the scale are 29 and 145, respectively. Higher total scores reflect healthier and better-quality peer relationships.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Marmara University, Faculty of Health Sciences | Maltepe | Istanbul |
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Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07723040 on ClinicalTrials.gov ↗ ← All trials in Turkey