The Effect of a Self-Compassion-Based Mindfulness Psychoeducation Program on Perceived Stress and Continuous Hope Among Healthcare Students (SCBMP-HS)
The Effect of a Self-Compassion-Based Mindfulness Psychoeducation Program on Perceived Stress Levels and Levels of Continuous Hope Among Healthcare Students: A Randomized Controlled Trial
The aim of this study is to evaluate the effect of a 6-week self-compassion-based mindfulness psychoeducation program on perceived stress and continuous hope among healthcare students.
This study was designed as a single-blind, randomized controlled trial and was conducted during the spring semester of the 2024-2025 academic year among students enrolled in the Health Care Services Department at Trabzon University Tonya Vocational School. A total of 60 students who met the eligibility criteria and voluntarily agreed to participate were included in the study and randomly assigned to the intervention or control group.
The intervention group received a 6-week self-compassion-based mindfulness psychoeducation program, while the control group did not receive the psychoeducational intervention during the study period. Data were collected using a Demographic Information Form, the Perceived Stress Scale, and the Continuous Hope Scale. Perceived stress and continuous hope were assessed at baseline and at Week 6, immediately after completion of the intervention. Study data were analyzed using SPSS version 22.0.
Przegląd badań
Status
Warunki
Interwencja / Leczenie
Typ studiów
Zapisy (Rzeczywisty)
Faza
- Nie dotyczy
Kontakty i lokalizacje
Lokalizacje studiów
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Tonya
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Trabzon, Tonya, Turcja (Türkiye), 61000
- Tonya Vocational School
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dorosły
- Starszy dorosły
Akceptuje zdrowych ochotników
Opis
Inclusion Criteria:
- Currently enrolled in the Department of Health Care Services
- Aged 18 years or older
- Willing to participate in the study and provide informed consent
- Able to read and understand Turkish
- No current psychiatric diagnosis and not receiving active psychiatric treatment
- No participation in a mindfulness-, self-compassion-, or stress management-based psychoeducational program within the previous six months
Exclusion Criteria:
- Current psychiatric diagnosis or active psychiatric treatment
- Previous participation in a self-compassion- or mindfulness-based psychoeducational program within the previous six months
- Inability to read and understand Turkish
- Refusal to provide informed consent
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie podtrzymujące
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
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Eksperymentalny: Self-Compassion-Based Mindfulness Psychoeducation Group
Participants in the intervention group received a 6-week Self-Compassion-Based Mindfulness Psychoeducation Program delivered through in-person group sessions at Trabzon University Tonya Vocational School. The program consisted of six sessions delivered once weekly. Participants were divided into three subgroups of 10 participants for the delivery of the program. Each session was conducted by the researcher according to the structured psychoeducation program and lasted approximately 45-90 minutes. The program included psychoeducational content and exercises focused on self-compassion, mindfulness, stress awareness, emotion regulation, and self-compassion-based coping skills. |
The Self-Compassion-Based Mindfulness Psychoeducation Program was delivered through in-person group sessions at Trabzon University Tonya Vocational School. The program consisted of six sessions delivered once weekly. Participants in the intervention group were divided into three subgroups of 10 participants. Each session was conducted by the researcher according to the structured psychoeducation program and lasted approximately 45-90 minutes. The program included psychoeducational content and exercises focused on self-compassion, mindfulness, stress awareness, emotion regulation, and self-compassion-based coping skills. |
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Brak interwencji: No-Intervention Control Group
Participants in the control group did not receive the Self-Compassion-Based Mindfulness Psychoeducation Program during the 6-week study period.
After completion of the post-intervention assessment, participants in the control group were offered a single-session breathing exercise training.
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Change in Trait Hope Scale Total and Subscale Scores
Ramy czasowe: Baseline and Week 6 (immediately after completion of the intervention)
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Hope is assessed using the Trait Hope Scale, a 12-item measure consisting of two subscales: Agency Thinking and Pathways Thinking.
Four items are filler items and are not included in scoring.
Higher total scores indicate higher levels of hope.
The scale is administered at baseline and at Week 6, immediately after completion of the psychoeducation program, to assess change in hope over time.
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Baseline and Week 6 (immediately after completion of the intervention)
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
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Change in Perceived Stress Scale Total and Subscale Scores
Ramy czasowe: Baseline and Week 6 (immediately after completion of the intervention)
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Perceived stress is assessed using the 8-item Perceived Stress Scale.
The scale includes two subscales: Perceived Stress and Perceived Coping.
Items are rated on a 5-point Likert scale from 0 to 4, and the total score ranges from 0 to 32.
Higher total scores indicate higher levels of perceived stress.
The scale is administered at baseline and at Week 6, immediately after completion of the psychoeducation program, to assess change in perceived stress over time.
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Baseline and Week 6 (immediately after completion of the intervention)
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Współpracownicy i badacze
Sponsor
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Inne numery identyfikacyjne badania
- 2025-584
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Opis planu IPD
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
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