NCT05312749

Brief Summary

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)".

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
66

participants targeted

Target at P25-P50 for not_applicable anxiety

Timeline
Completed

Started Sep 2021

Shorter than P25 for not_applicable anxiety

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 27, 2021

Completed
28 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 25, 2021

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 25, 2021

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

March 16, 2022

Completed
20 days until next milestone

First Posted

Study publicly available on registry

April 5, 2022

Completed
Last Updated

April 11, 2022

Status Verified

April 1, 2022

Enrollment Period

28 days

First QC Date

March 16, 2022

Last Update Submit

April 4, 2022

Conditions

Outcome Measures

Primary Outcomes (2)

  • The State-Trait Anxiety Inventory

    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

    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.

    12 week

Study Arms (2)

Experimental:

EXPERIMENTAL

Experimental: will do progressive relaxation exercises

Other: progressive relaxation exercises

Control

NO INTERVENTION

won't do progressive relaxation exercises

Interventions

progressive relaxation exercises

Also known as: progressive muscle relaxation exercises
Experimental:

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Being over 18 years old
  • Studying in the 2021-2022 academic year
  • Being in 2nd grade
  • Not going into clinical practice before

You may not qualify if:

  • Being under the age of 18
  • Not studying in the 2021-2022 academic year
  • Being in 1st, 3rd or 4th grade
  • Prior clinical practice

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Atatürk university nursing faculty

Erzurum, Center, 25240, Turkey (Türkiye)

Location

Fırat Üniversitesi

Elâzığ, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Anxiety Disorders

Condition Hierarchy (Ancestors)

Mental Disorders

Study Officials

  • Gülcan B.TURAN, PH

    Firat University

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
INVESTIGATOR
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

March 16, 2022

First Posted

April 5, 2022

Study Start

September 27, 2021

Primary Completion

October 25, 2021

Study Completion

December 25, 2021

Last Updated

April 11, 2022

Record last verified: 2022-04

Data Sharing

IPD Sharing
Will not share

The article is intended to be shared after it is published.

Locations