- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07781813
Progressive Muscle Relaxation and Stress in Nursing Students
Effect of Progressive Muscle Relaxation on Perceived Stress Among Nursing Students During Psychiatric Nursing Clinical Practice: A Quasi-Experimental Study
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
This quasi-experimental study was conducted with fourth-year nursing students enrolled in the Psychiatric and Mental Health Nursing course at KTO Karatay University. The study used a pretest-posttest control group design. Students were allocated to intervention and control groups according to their positions on the official class attendance list; students with odd-numbered positions formed one group and those with even-numbered positions formed the other group. The intervention group was determined by a random selection from sealed envelopes labeled "odd numbers" and "even numbers." A total of 60 students participated in the study, with 30 students in each group.
Baseline data were collected using a Student Information Form and the Perceived Stress Scale for Nursing Students. Following the pretest assessment, students in the intervention group participated in progressive muscle relaxation sessions once a week for five weeks. Each session lasted approximately 30-40 minutes and included diaphragmatic breathing and systematic tensing and relaxing of major muscle groups under the verbal guidance of the researcher. Students in the control group continued their usual routines and received no relaxation training or additional intervention during the study period.
At the end of the five-week intervention period, the Perceived Stress Scale for Nursing Students was readministered to both groups. Pretest and posttest perceived stress scores were compared within and between groups to evaluate the effect of the progressive muscle relaxation intervention.
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
-
-
-
Konya, Tyrkiet (Türkiye), 42020
- KTO Karatay University
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
- Aged 18 years or older
- Enrolled in the Psychiatric and Mental Health Nursing course
- Regular attendance in the course
- Willing to participate regularly in progressive muscle relaxation exercises if allocated to the intervention group
Exclusion Criteria:
- Repeating the Psychiatric and Mental Health Nursing course
- Receiving treatment for a mental health disorder
- Having a physical condition or disability that could prevent participation in progressive muscle relaxation exercises
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Progressive Muscle Relaxation Group
Participants in this group received progressive muscle relaxation (PMR) sessions administered by the researcher once a week for five weeks.
Each session lasted approximately 30-40 minutes.
|
Participants in the intervention group received progressive muscle relaxation (PMR) once a week for five weeks.
Each session lasted approximately 30-40 minutes.
During the first session, participants received brief instruction on PMR and diaphragmatic breathing.
Under the researcher's verbal guidance, participants systematically tensed each major muscle group for approximately 5-7 seconds and then relaxed it.
The same protocol was repeated weekly for five weeks under similar conditions.
|
|
Ingen indgriben: Control Group
Participants in the control group continued their usual routines and received no relaxation training or additional intervention during the study period.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Perceived Stress Level
Tidsramme: Baseline and immediately after the 5-week intervention
|
Perceived stress was assessed using the Perceived Stress Scale for Nursing Students (PSSNS).
The scale consists of 29 items across six subscales.
Each item is rated from 0 (not stressful for me) to 4 (extremely stressful for me), yielding a total score ranging from 0 to 116.
Higher scores indicate higher levels of perceived stress.
|
Baseline and immediately after the 5-week intervention
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Stress From Lack of Professional Knowledge and Skills
Tidsramme: Baseline and immediately after the 5-week intervention
|
This subscale of the Perceived Stress Scale for Nursing Students (PSSNS) consists of 3 items (items 2, 7, and 11).
Each item is rated from 0 to 4, yielding a subscale score ranging from 0 to 12. Higher scores indicate higher perceived stress related to lack of professional knowledge and skills.
|
Baseline and immediately after the 5-week intervention
|
|
Stress From Taking Care of Patients
Tidsramme: Baseline and immediately after the 5-week intervention
|
This subscale of the Perceived Stress Scale for Nursing Students (PSSNS) consists of 8 items (items 1, 4, 6, 8, 10, 12, 14, and 19).
Each item is rated from 0 to 4, yielding a subscale score ranging from 0 to 32.
Higher scores indicate higher perceived stress related to patient care.
|
Baseline and immediately after the 5-week intervention
|
|
Stress From Assignments and Workload
Tidsramme: Baseline and immediately after the 5-week intervention
|
This subscale of the Perceived Stress Scale for Nursing Students (PSSNS) consists of 5 items (items 3, 9, 13, 17, and 21).
Each item is rated from 0 to 4, yielding a subscale score ranging from 0 to 20.
Higher scores indicate higher perceived stress related to assignments and workload.
|
Baseline and immediately after the 5-week intervention
|
|
Stress From Teachers and Nursing Staff
Tidsramme: Baseline and immediately after the 5-week intervention
|
This subscale of the Perceived Stress Scale for Nursing Students (PSSNS) consists of 6 items (items 15, 16, 18, 20, 25, and 27).
Each item is rated from 0 to 4, yielding a subscale score ranging from 0 to 24.
Higher scores indicate higher perceived stress related to teachers and nursing staff.
|
Baseline and immediately after the 5-week intervention
|
|
Stress From the Environment
Tidsramme: Baseline and immediately after the 5-week intervention
|
This subscale of the Perceived Stress Scale for Nursing Students (PSSNS) consists of 3 items (items 5, 23, and 26).
Each item is rated from 0 to 4, yielding a subscale score ranging from 0 to 12. Higher scores indicate higher perceived stress related to the clinical environment.
|
Baseline and immediately after the 5-week intervention
|
|
Stress From Peers and Daily Life
Tidsramme: Baseline and immediately after the 5-week intervention
|
This subscale of the Perceived Stress Scale for Nursing Students (PSSNS) consists of 4 items (items 22, 24, 28, and 29).
Each item is rated from 0 to 4, yielding a subscale score ranging from 0 to 16.
Higher scores indicate higher perceived stress related to peers and daily life.
|
Baseline and immediately after the 5-week intervention
|
Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Ledende efterforsker: Özden Gülal, MSc, Selcuk University, Aksehir Faculty of Health Sciences
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
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
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- KaratayUN
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
IPD-planbeskrivelse
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .