The Effect of Progressive Relaxation Exercises on the Sleep Quality of Nursing Students

February 3, 2025 updated by: seher ÇEVİK, Inonu University

The Effect of Progressive Relaxation Exercises Administered Via Telenursing on the Sleep Quality of Nursing Students After the Earthquake in Turkey

Aim: The study aims to examine the effect of progressive relaxation exercises administered to nursing students via telenursing on sleep quality after the February 6 earthquake in Turkey.

Materials and Methods: The study was conducted as a randomized controlled study. The study population consisted of first-, second-, and third-year nursing students enrolled in the nursing departments of two universities located in eastern Turkey, who were residing in one of the 11 cities affected by the earthquake during the February 6 Turkey earthquake. The sample included 86 students (40 experimental, 46 control). While the control group received no intervention, the experimental group received progressive relaxation exercises for 20 minutes every night for 4 weeks, 1 hour before the routine bedtime (or the time they planned to go to sleep) by making a video call (via Google Meet application) with the student. Data were collected using a personal information form and the Pittsburgh Sleep Quality Scale. Descriptive statistical methods (frequency, percentage, arithmetic mean, standard deviation), independent groups t-test, and paired t-test were used to evaluate the data.

Conclusion: The research results can showed that progressive relaxation exercises could be an effective intervention in improving sleep quality after an earthquake. Additionally, conducting these exercises via telenursing could contribute significantly to the sustainability and control of the intervention.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

  • If the students have any pre-sleep habits (using aromatic oil, massage, listening to music, etc.) that they routinely practice and that may affect the results of the study, they will be asked not to do so for 6 weeks.
  • A video call is made with the students.
  • The procedure is explained to the patient and any questions are answered or concerns are addressed.
  • If possible, the patient is asked to move to a ventilated room away from noise so that the procedure can be performed comfortably and not interrupted.
  • Procedure
  • It is explained to the individual that the procedure can be done sitting or lying down and he/she is asked to release his/her muscles and take a comfortable position.
  • The individual is asked to close his/her eyes and focus only on his/her body.
  • For 5 seconds, the individual is asked to take a slow deep breath.
  • He/she is asked to breathe out in a controlled manner in 3-4 seconds.
  • The process of taking a deep breath in 5 seconds and giving it back in 3-4 seconds is repeated 3 times.
  • While breathing, the individual is asked to squeeze his/her forehead muscles by raising his/her eyebrows as high as possible at the same time.
  • After 10 seconds of tightening the forehead muscles, the patient is asked to slowly lower his/her eyebrows and slowly relax and release the forehead muscles while exhaling. He/she is encouraged to feel the relaxation in the forehead muscles.
  • The individual is asked to take a deep breath, close his/her eyes tightly and squeeze the muscles around the eyes.
  • After 10 seconds of tightening the muscles around the eyes, he/she is asked to slowly relax and release the muscles around the eyes while exhaling. With muscle

Study Type

Interventional

Enrollment (Actual)

86

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Center
      • Malatya, Center, Turkey, 44100
        • Inonu University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • The study included students who were in one of the 11 cities affected by the Turkey earthquake,
  • did not have a medical diagnosis related to sleep disorders,
  • were not using any sleep medications or long-acting treatments,
  • had access to necessary equipment for telenursing such as the internet, computer, or phone,
  • were enrolled in the first, second, or third year of the nursing program.

Exclusion Criteria:

  • The fourth-grade nursing students were excluded from the study because they undergo internship training and work night shifts,
  • which may affect their sleep patterns and quality and create a difference between them and other students.
  • Students with any diagnosis related to sleep and those with any psychiatric diagnosis were also excluded.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Single Group Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention

Progressive relaxation exercises were conducted by the researcher, who had received training in this area. The students were informed in detail about the study's implementation process.

For the next 4 weeks, every night, 1 hour before the routine bedtime (or the time when the student planned to sleep), a video call (via the Google Meet application) was made with the student, and progressive relaxation exercises were performed. The exercise took approximately 20 minutes and followed the implementation protocol (Davis et al., 2008; Payne, 2000). Group interviews were conducted for students with similar sleep hours. They were asked to move to a ventilated room away from noise so that the exercises could be practiced comfortably and not interrupted.

For the next 4 weeks, every night, 1 hour before the routine bedtime (or the time when the student planned to sleep), a video call (via the Google Meet application) was made with the student, and progressive relaxation exercises were performed. The exercise took approximately 20 minutes and followed the implementation protocol (Davis et al., 2008; Payne, 2000). Group interviews were conducted for students with similar sleep hours. They were asked to move to a ventilated room away from noise so that the exercises could be practiced comfortably and not interrupted.
Other Names:
  • Progressive relaxation exercises practice
No Intervention: control
No intervention was applied to the control group in the study. Data collection forms were filled out only at the beginning and in the fourth week of the study.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pittsburgh Sleep Quality Index
Time Frame: 3 month
Pittsburgh Sleep Quality Index The scale was developed by Buysse et al. and validated in Turkish by Agargün et al. (Buysse et al., 1989; Agargün, 1996). Of the 24 items on the scale, 18 are included in the evaluation. The scale consists of 7 sub-dimensions: Subjective Sleep Quality, Sleep Latency, Sleep Duration, Habitual Sleep Efficacy, Sleep Disturbances, Use of Sleep Medication, and Daytime Dysfunction. Each sub-dimension is scored between 0-3, and the total scale score ranges from 0 to 21. An increase in the scale score indicates a decline in sleep quality. The results are evaluated in three categories: 0-5 points indicate healthy sleep, 6-10 points indicate poor sleep, and above 10 points indicate chronic sleep disturbance. The Cronbach's alpha internal consistency coefficient for the scale was calculated as 0.80 by Ağargün (1996).
3 month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 1, 2023

Primary Completion (Actual)

February 15, 2024

Study Completion (Actual)

March 30, 2024

Study Registration Dates

First Submitted

January 25, 2025

First Submitted That Met QC Criteria

February 3, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 3, 2025

Last Verified

February 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • seher CEVİK AKTURA

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Participants' data were collected for research purposes only according to the ethical principle of condentiality and protection. Therefore, it cannot be shared.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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