Cognitive Behavior Therapy for Social Media Addiction, Insomnia, and Family Relationship Among Individuals With Social Media Addiction: A Randomized Control Tria

December 19, 2023 updated by: Qasir Abbas, Government College University Faisalabad

Objectives This study is designed to investigate the following objectives To manage the social media addiction in order to improve lifestyle, attitude and family relations of the individuals and explore related psychological problems which can arise because of this addiction.

To explore the effectiveness of cognitive behaviour therapy (CBT) in the management of social media addiction in individuals which is decreasing the health of their lifestyle, attitude and family bonding.

To explain how abusive use of social media can increase the risk of psychological and behavioural problems.

Study Overview

Status

Active, not recruiting

Detailed Description

A sample of 150 individuals (male and female N=150) was recruited from different universities of Faisalabad for the purpose. A strategy of non-probability sampling of purposive technique was used for the recruitment of sample. The age range for the sample will be 18-22 as young adults and adults was targeted. Firstly individuals were screened out through social media addiction scale from which (n=60) participants were excluded because they did not meet the inclusion criteria of the study. Some participants left because lack of interest. After excluding (n=60) from the study rest of the participants (n=90) were randomized and allocated to experimental (n=45) and control group (n=45). After allocation of participants in the relevant group some participants were lost from the follow up from experimental (n=21) due to decline to participate and control group (n=20) due to lack of interest. Final analysis was conducted on experimental group and (n=24) control group (n=25) for the study.

Study Type

Interventional

Enrollment (Estimated)

150

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

    • Punjab
      • Faisalābad, Punjab, Pakistan, 38000
        • Qasir Abbas

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:

  • Individuals screened out through social media addiction scale will be used for the experimental study. Both male and female participants will be taken for the study. People with even mild score on social media addiction will be considered eligible for the study. Only people in the age range of 18-22 will be taken as participants in the study

Exclusion Criteria:

  • Individuals not within the age range of 18-22 will not be taken as participants.

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: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Arms of the study
Experimental group : participants in experimental group will receive 8-10 sessions of intervention in overall the course of study.
Cognitive behavioral therapy-based interventions were used to manage social media addiction and; to address associated problems with it. Psychoeducation, problem conceptualization, cognitive distortions and belief identification,Time management,Stress and distress management, Emotional and beliefs modification,Priority and Goal setting, Problem solving skills, Social skill training, Emotional and behavioral activation and Relapse prevention are techniques that will be used in the intervention.
No Intervention: Control group
Control group: participants in control group will not receive any sessions of intervention.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Social Media Addiction
Time Frame: 4 months
Social media addiction scale was used to screen out the participants for eligibility assessment. Participants who will score high on the social media addiction scale will be enrolled
4 months
Insomnia severity index
Time Frame: 4
This is 27 item scale which assess the quality of sleep.
4
Family relationship scale
Time Frame: 4
Family relationship scale will be used to assess the person and family bonding and it will assess the impact of social media addiction
4

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Attitude and Belief Scale
Time Frame: 4
This scale will assess the person general attitude and belief when he/she is using social media and being dependant
4

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Qasir Abbas, PHD, Government College University Faisalabad

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)

November 15, 2023

Primary Completion (Estimated)

February 1, 2024

Study Completion (Estimated)

April 10, 2024

Study Registration Dates

First Submitted

November 29, 2023

First Submitted That Met QC Criteria

December 19, 2023

First Posted (Actual)

January 3, 2024

Study Record Updates

Last Update Posted (Actual)

January 3, 2024

Last Update Submitted That Met QC Criteria

December 19, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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