The Effect of Web Based Progressive Muscle Relaxation Exercise on Clinical Stress and Anxiety of Nursing Students
4. april 2022 opdateret af: gülcan bahcecioğlu, Ataturk University
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)".
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
66
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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-
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Elazığ, Kalkun
- Fırat Üniversitesi
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Center
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Erzurum, Center, Kalkun, 25240
- Atatürk university nursing faculty
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
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
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
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 |
|---|---|
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Eksperimentel: Experimental:
Experimental: will do progressive relaxation exercises
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progressive relaxation exercises
Andre navne:
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Ingen indgriben: Control
won't do progressive relaxation exercises
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
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.
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12 week
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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
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Studieleder: Gülcan B.TURAN, PH, Firat University
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
27. september 2021
Primær færdiggørelse (Faktiske)
25. oktober 2021
Studieafslutning (Faktiske)
25. december 2021
Datoer for studieregistrering
Først indsendt
16. marts 2022
Først indsendt, der opfyldte QC-kriterier
28. marts 2022
Først opslået (Faktiske)
5. april 2022
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
11. april 2022
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
4. april 2022
Sidst verificeret
1. april 2022
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 2021/09-45
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Ingen
IPD-planbeskrivelse
The article is intended to be shared after it is published.
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
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