- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06674746
Effect of Solution-Focused Approach on the Internet,Social Media Addiction and Self-Efficacy Levels OfNursing Students
November 3, 2024 updated by: Taha Yasir Mert, Cumhuriyet University
The Effect of Solution-Focused Approach on the Internet, Social Media Addiction and Self-Efficacy Levels of Nursing Students
The purpose of this research; is to determine the effect of solution-oriented approach on internet, social media addiction and self-efficacy levels of nursing students.
A pretest-posttest randomized controlled experimental design will be used in the research.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
The research will be carried out between 4 April 2022 and 28 April 2023 at Sivas Cumhuriyet University .
Personal Information Form, Internet Addiction Scale, Social Media Addiction Scale and Self-Efficacy Competence Scale were applied to a total of 1057 nursing students who were continuing their education in the 1st, 2nd and 3rd years at the Faculty of Health Sciences (683) and Suşehri Health College (374), where the research would be conducted.Since the final data of the study will be received next year, students in the 1st, 2nd and 3rd grades will be included in the interviews in order to prevent data loss, and 4th graders will be excluded from the study.
Study Type
Interventional
Enrollment (Actual)
60
Phase
- Not Applicable
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:
- Being between the ages of 18-25,
- 67 < Internet Addiction Scale (IAS) Score < 109,
- 73 < Social Media Addiction (SMDS) Score < 140.
Exclusion Criteria:
- Receiving any psychological counseling and treatment,
- Being closed to communication,
- To have extended the term,
- Not volunteering to participate in the research.
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: Prevention
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: intervention
Using the simple random numbers table from the population in the risk group, 60 randomly selected students will be randomly assigned to the experimental and control groups as 30 students.
A two-stage stratified random method will be used in order to make assignments to the intervention and control groups equally and homogeneously.
Firstly; The class and gender strata determined by scanning the literature will be created.
Afterwards, each class and the male and female students in these classes will be determined.
Then, the students in each stratum will be assigned to the intervention and control groups according to the two-layer random method, one intervention and one control.
|
The interviews with the control group were planned as eight sessions.
There will be defined time intervals between sessions.
It is estimated to take 6 months.
|
|
No Intervention: control
Using the simple random numbers table from the population in the risk group, 60 randomly selected students will be randomly assigned to the experimental and control groups as 30 students.
A two-stage stratified random method will be used in order to make assignments to the intervention and control groups equally and homogeneously.
Firstly; The class and gender strata determined by scanning the literature will be created.
Afterwards, each class and the male and female students in these classes will be determined.
Then, the students in each stratum will be assigned to the intervention and control groups according to the two-layer random method, one intervention and one control.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Internet Addiction Scale
Time Frame: 10 minute
|
Developed by Günç and Kayri (2010), the İBÖ is in the five-point likert type, and the likert-style expressions are; "Strongly Agree", "Agree", "Undecided", "Disagree", "Strongly Disagree".
|
10 minute
|
|
Social Media Addiction Scale
Time Frame: 10 minute
|
The Social Media Addiction Scale was developed by Tutgun-Ünal and Deniz (2015) in order to measure the social media addiction of university students and all validity and reliability studies were carried out.
Consisting of 41 items and four factors (occupation, mood regulation, repetition, and conflict), SMDS is a 5-point Likert-type scale graded as "Always", "Often", "Sometimes", "Rarely" and "Never".
|
10 minute
|
|
Self-Efficacy-Efficacy Scale
Time Frame: 5 minute
|
The Self-Efficacy Efficiency scale, developed by Sherer et al. (1982) and adapted into Turkish by Gözüm and Aksayan (1999), is a 5-point Likert-type scale and includes 23 items.
The cronbach alpha internal consistency coefficient of the Turkish version of the scale was found to be .81
(Gözüm & Aksayan, 2010).
|
5 minute
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Taha Mert, postgraduate, Cumhuriyet University
- Study Director: Nuran Güler, professor, Cumhuriyet University
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)
May 26, 2023
Primary Completion (Actual)
October 24, 2023
Study Completion (Actual)
October 24, 2023
Study Registration Dates
First Submitted
September 16, 2022
First Submitted That Met QC Criteria
November 3, 2024
First Posted (Estimated)
November 5, 2024
Study Record Updates
Last Update Posted (Estimated)
November 5, 2024
Last Update Submitted That Met QC Criteria
November 3, 2024
Last Verified
November 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 17082022
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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