- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05993988
The Effect of Telerehabilitation on Clinical Stress Level and Stress Responses in Nursing Students
August 12, 2023 updated by: Mustafa Savaş Torlak, KTO Karatay University
The Effect of Telerehabilitation Practice on the Clinical Stress Level and Stress Responses of Nursing Students During Their First Clinical Experience
It was aimed to examine the effect of telerehabilitation on clinical stress level and stress responses in nursing students.
Study Overview
Detailed Description
It was aimed to examine the effect of telerehabilitation on clinical stress level and stress responses in nursing students.There is no study in the literature examining the relationship between telerehabilitation and clinical stress in nursing students.
Since our study will be the first to investigate the subject, we foresee that it is scientifically important and will shed light on future studies.
In addition, national or international publications are planned after the study is completed.
Study Type
Interventional
Enrollment (Actual)
75
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
-
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Eyalet/Yerleşke
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Karatay, Eyalet/Yerleşke, Turkey, 42000
- Mustafa Savaş Torlak
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-
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
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- to be between the ages of 18-24
- to do the first clinical internship in the hospital
Exclusion Criteria:
- have joint limitation
- have congenital anomaly
- have any orthopedic problem
- have any serious psychological problems
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: control group
The participants in the control group did not receive any intervention.
|
|
|
Experimental: Exercise group
The participants in the exercise group performed Jacobson muscle relaxation exercises with a specialist physiotherapist through the Zoom program (https://zoom.us).
The exercises were applied 4 days a week for 4 weeks.
|
Muscle relaxing Technique
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perceived Stress Scale for Nursing Students
Time Frame: baseline and 4 weeks
|
Sheu et al. (2002) originally in Chinese, the scale consists of 29 items.Total score; It ranges from 0 to 116.
A high score indicates a high level of stress.
The internal consistency coefficient value of the original scale is 0.86.
|
baseline and 4 weeks
|
|
Biopsychosocial Response Scale of Nursing Students
Time Frame: baseline and 4 weeks
|
The scale was developed by Sheu et al. (2002).
There are 21 items in the scale.Total score; It ranges from 0 to 84 (sub-dimension total scores are 32, 28, and 24 points, respectively).
High score indicates more symptom presence and poor bio-psycho-social status.
|
baseline and 4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
April 1, 2023
Primary Completion (Actual)
May 1, 2023
Study Completion (Actual)
June 1, 2023
Study Registration Dates
First Submitted
August 4, 2023
First Submitted That Met QC Criteria
August 12, 2023
First Posted (Actual)
August 16, 2023
Study Record Updates
Last Update Posted (Actual)
August 16, 2023
Last Update Submitted That Met QC Criteria
August 12, 2023
Last Verified
August 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- Karatayanxiety
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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