- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07245862
Evaluation of a Family-centered Program for Problematic Gaming/Excessive Screen Use (S-FAME)
April 24, 2026 updated by: Region Skane
Evaluation of a Family-centered Program for Problematic Gaming/Excessive Screen Use in a Child and Adolescent Population Within Social Services in Light of the New Social Services Law
The Family-Centered Program for Problematic Gaming and Excessive Screen Use (FAME) is a pioneering initiative designed to address the growing challenges of excessive screen use and gaming among children and adolescents, particularly within family dynamics.
Study Overview
Status
Recruiting
Detailed Description
The Family-Centered Program for Problematic Gaming and Excessive Screen Use (FAME) is a pioneering initiative designed to address the growing challenges of excessive screen use and gaming among children and adolescents, particularly within family dynamics.
With digital media becoming one of the most prevalent leisure activities, excessive use has been linked to adverse outcomes, including depression, sleep disturbances, and family conflicts.
Despite these concerns, there are no evaluated family-centered interventions in Sweden that address these issues comprehensively.
This randomized controlled trial (RCT) aims to evaluate the effectiveness and feasibility of the S-FAME program, developed in collaboration with social services across two municipalities (Lund, Eslöv).
The program integrates psychoeducation, cognitive restructuring, and social-emotional learning, focusing on both children and their families.
It acknowledges that problematic screen use often develops within family contexts and aims to improve parenting practices and enhance parent-child relationships.
The project aligns with the new Social Services Act, which will come into effect in July 2025, emphasizing easily accessible, preventive, and low-threshold interventions-so-called non-means-tested services.
By targeting both individual and family needs, the intervention has the potential to reduce societal costs, enhance family well-being, and address health inequalities.
With its innovative and scalable design, S-FAME provides a much-needed framework to tackle one of today's most pressing challenges in youth development- excessive screen use.
We are a team of researchers with great experience in research as well as clinical work in the field of adolescence, social work and ANDTS (Alkohol, narkotika, droger, tobak och spel).
The project is well established within the School of Social Sciences/Medical Faculty at Lund University, as well as within the innovation and development departments of two social services units.
PI Emma Claesdotter-Knutsson (ECK), associate professor and senior consultant in child and adolescent psychiatry at Lund University/Region Skåne with major research areas of gaming, gambling and screens use.
ECK has extensive clinical expertise and has played a key role at the Swedish Public Health Agency, contributing to the development of recommendations on child digital media use.
PI ECK brings extensive experience and formal training in leading collaborative projects.
Study Type
Interventional
Enrollment (Estimated)
170
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 Contact
- Name: Emma Claesdotter-Knutsson, PhD
- Phone Number: +46768871765
- Email: emma.claesdotter-knutsson@skane.se
Study Contact Backup
- Name: Sabina Kapetanovic, PhD
- Email: sabina.kapetanovic@hv.se
Study Locations
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-
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Lund, Sweden
- Recruiting
- Child and Adolescent Psychiatry Clinic
-
Contact:
- Emma Claesdotter-Knutsson, MD; PhD
- Phone Number: 0046768871765
- Email: emma.claesdotter-knutsson@med.lu.se
-
-
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
- Child
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- family conflicts related to screen use
- spaeks and udnerstand swedish
Exclusion Criteria:
- se above
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 |
|---|---|
|
Active Comparator: Intervention
The critical components include psychoeducation, cognitive restructuring, and social and emotional learning.
The goals are to help children and parents understand the positive and negative aspects of screen use and to prevent related problems and family conflicts.
The intervention consist of 4 group mettings parents and children separate.
Max 10 children per group
|
The critical components include psychoeducation, cognitive restructuring, and social and emotional learning.his
would be the first intervention offering help for both children and their parents.
Such an intervention could be beneficial not only to individual families, but also to society at large by reducing societal costs, enhancing family well-being, and addressing health inequalities .
the intervention is agroup intervention in 4 sessions with parents in one group and children in one group.
The goals are to help children and parents understand the positive and negative aspects of screen use and to prevent related problems and family conflicts.
T
|
|
Active Comparator: Control
This group will recieve treatment as usual.
After final follow up this group will be offered an online parental intervention of 3 sessions
|
This group will recieve TAU == treat ment as usual depending on the practice at the Social service they belong to
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
FCU
Time Frame: Baseline; Post treatment; 1 month post treatment
|
five items measure parent-child warmth, and three items measure parent-child conflicts
|
Baseline; Post treatment; 1 month post treatment
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
SCREENS-Q (adapted) time (19) • PARCA for assessing aspects of parent-child relationship and parenting practices (22) • FCU five items measure parent-child warmth, and three items measure parent-child conflicts (23)
Time Frame: Baseline; Post treatment; 1 month post treatment
|
screening form, for valuing children and adolescent´s screen time screening form, for valuing children and adolescent´s screen time screening form, for valuing children and adolescent´s screen time
|
Baseline; Post treatment; 1 month post treatment
|
|
PARCA
Time Frame: Baseline; Post treatment; 1 month post treatment
|
for assessing aspects of parent-child relationship and parenting practices
|
Baseline; Post treatment; 1 month post treatment
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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)
January 1, 2026
Primary Completion (Estimated)
January 1, 2027
Study Completion (Estimated)
January 1, 2028
Study Registration Dates
First Submitted
September 12, 2025
First Submitted That Met QC Criteria
November 17, 2025
First Posted (Actual)
November 24, 2025
Study Record Updates
Last Update Posted (Actual)
April 30, 2026
Last Update Submitted That Met QC Criteria
April 24, 2026
Last Verified
November 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2025-05262-01
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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