- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT05312749
The Effect of Web Based Progressive Muscle Relaxation Exercise on Clinical Stress and Anxiety of Nursing Students
The Effect of Web-Based Progressive Muscle Relaxation Exercise on the Perceived Stress and Anxiety Level of Nursing Students Found in Clinical Practice for the First Time: A Randomized Controlled Trial
Purpose: The study was conducted to examine the effect of web-based progressive muscle relaxation exercise on the perceived stress and anxiety level of nursing students who were in clinical practice for the first time.
Method: This randomized controlled study was conducted at a state university in Turkey. The sample of the study consisted of a total of 66 nursing students, 36 of whom were control and 30 interventions, who were educated in the 2021-2022 academic year, were in clinical practice for the first time and agreed to participate in the research. The intervention group was asked to perform a total of 36 sessions of progressive muscle relaxation exercise, 3 days a week for 12 weeks. Data; It was collected using the "Sociodemographic Characteristics Form", "State-Trait Anxiety Inventory (DSQ)" and "Perceived Stress Inventory (PSI)".
Studieoversikt
Status
Intervensjon / Behandling
Studietype
Registrering (Faktiske)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiesteder
-
-
-
Elazığ, Tyrkia
- Fırat Üniversitesi
-
-
Center
-
Erzurum, Center, Tyrkia, 25240
- Atatürk university nursing faculty
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-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- Being over 18 years old
- Studying in the 2021-2022 academic year
- Being in 2nd grade
- Not going into clinical practice before
Exclusion Criteria:
- Being under the age of 18
- Not studying in the 2021-2022 academic year
- Being in 1st, 3rd or 4th grade
- Prior clinical practice
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: Experimental:
Experimental: will do progressive relaxation exercises
|
progressive relaxation exercises
Andre navn:
|
Ingen inngripen: Control
won't do progressive relaxation exercises
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
The State-Trait Anxiety Inventory
Tidsramme: 12 week
|
The State-Trait Anxiety Inventory was developed by Spielberger et al. (1970) (Spielger, Gorsuch, & Lushene, 1970).
The validity and reliability of the scale in Turkey was established by Öner and Le Compte (1983) (Öner & Le Compte, 1983).
The scale consists of two parts, the State Anxiety Inventory and the Trait Anxiety Inventory.
The first 20 items assess situational anxiety, and the last 20 items assess trait anxiety.
In this study, the "State Anxiety Inventory", which is the first 20 items, was used to evaluate situational anxiety.
State Anxiety Scale; It was developed to determine how an individual feels at a certain moment and under certain conditions.
The scale is 4-point Likert type.
Scores from the scale range from 20 to 80. Higher scores indicate higher levels of anxiety.
|
12 week
|
Perceived Stress Scale
Tidsramme: 12 week
|
The Perceived Stress Scale was developed by Cohen, Kamarck, and Mermelstein in 1983 to determine the level of stress that threatens human health (Cohen et al. 1983).
Its Turkish validity and reliability were determined by Eskin et al. (2013) (Eskin et al., 2013).
PSS-14 consists of 2 factors: "insufficient self-efficacy" and "stress" perception.
The scale is a 5-point Likert type scale and consists of 14 items.
As the scores obtained from the scale increase, the level of stress perceived by the person also increases.
PSS scores range from 0 to 56, with 0-35 point range indicating normal stress level and 35-56 point range indicating that the individual is under stress.
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12 week
|
Samarbeidspartnere og etterforskere
Sponsor
Etterforskere
- Studieleder: Gülcan B.TURAN, PH, Firat University
Publikasjoner og nyttige lenker
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
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
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 2021/09-45
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
IPD-planbeskrivelse
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .
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