- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07910032
Group Psychological Intervention to Reduce Distress Among Nursing Undergraduates
A Randomized Controlled Trial of Group Psychological Intervention to Reduce Distress Among Nursing Undergraduates
This is a randomized controlled trial. The study aims to explore the effect of group psychological intervention on academic distress among nursing undergraduates whose score on the self-developed Nursing Undergraduate Academic Distress Scale is ≥29. Eligible students will be randomly assigned to the intervention group or the control group. The intervention group will receive an 8-week structured group psychological intervention, while the control group will receive routine mental health education. The primary outcome is the change in academic distress score from baseline to the end of the 8-week intervention. Feasibility of the intervention program will also be evaluated.
Studieoversikt
Status
Forhold
Studietype
Registrering (Antatt)
Fase
- Ikke aktuelt
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- Full-time undergraduate nursing students;
- Achieved a score ≥29 on the self-developed Nursing Undergraduate Academic Distress Scale;
- Aged 18 years or above;
- Voluntarily participate in this study and signed written informed consent;
- Able to attend all 8-week group sessions and complete baseline and post-intervention assessments.
Exclusion Criteria:
- Diagnosed with mental disorders or receiving ongoing psychiatric treatment / psychological counseling;
- Participating in other similar psychological intervention programs at the same time;
- Unable to persist in the whole 8-week intervention and follow-up assessment due to personal reasons.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Støttende omsorg
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Enkelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Group psychological intervention
Participants will receive an 8-week structured group psychological intervention to alleviate psychological distress. |
8-week standardized group intervention program for alleviating psychological distress among nursing undergraduates. |
|
Aktiv komparator: Routine mental health education
Participants will receive routine general mental health education without the targeted distress intervention. |
General mental health science popularization education. |
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in psychological distress score
Tidsramme: Baseline, immediately after the 8-week intervention, and 1-month follow-up
|
The change score of psychological distress scale from baseline to post-intervention, which is used to compare the difference of psychological distress level between intervention group and control group. |
Baseline, immediately after the 8-week intervention, and 1-month follow-up
|
Samarbeidspartnere og etterforskere
Sponsor
Samarbeidspartnere
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Andre studie-ID-numre
- CMU-2026-Trial-01
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Legemiddel- og utstyrsinformasjon, studiedokumenter
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