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.
Studieoversigt
Status
Betingelser
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Ikke anvendelig
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
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 undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Støttende pleje
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: 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. |
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
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
|
Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- CMU-2026-Trial-01
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
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