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The Effect of a Self-Compassion-Based Mindfulness Psychoeducation Program on Perceived Stress and Continuous Hope Among Healthcare Students (SCBMP-HS)

19. august 2026 oppdatert av: Abdullah Usta, Ondokuz Mayıs University

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.

Studieoversikt

Studietype

Intervensjonell

Registrering (Faktiske)

60

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Tonya
      • Trabzon, Tonya, Tyrkia (Türkiye), 61000
        • Tonya Vocational School

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Ja

Beskrivelse

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

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Støttende omsorg
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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.

Ingen inngripen: 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.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in Trait Hope Scale Total and Subscale Scores
Tidsramme: Baseline and Week 6 (immediately after completion of the intervention)
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.
Baseline and Week 6 (immediately after completion of the intervention)

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in Perceived Stress Scale Total and Subscale Scores
Tidsramme: Baseline and Week 6 (immediately after completion of the intervention)
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.
Baseline and Week 6 (immediately after completion of the intervention)

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

1. mars 2025

Primær fullføring (Faktiske)

20. april 2025

Studiet fullført (Faktiske)

20. april 2025

Datoer for studieregistrering

Først innsendt

13. august 2026

Først innsendt som oppfylte QC-kriteriene

19. august 2026

Først lagt ut (Faktiske)

24. august 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

24. august 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

19. august 2026

Sist bekreftet

1. august 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • 2025-584

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

IPD-planbeskrivelse

I don't want to share it before it's published.

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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