Using Shared Decision Making to Improve Family Media Use Planning

April 22, 2026 updated by: Emily Kroshus, Seattle Children's Hospital
Investigators will conduct a pilot randomized controlled trial assessing the efficacy and feasibility of the newly developed Family Media Check-In (FMC).

Study Overview

Status

Recruiting

Conditions

Detailed Description

The clinical trial portion of this study will enroll 150 families (child age 11-17, and at least one parent/guardian). Stratified randomization will be used to assign families to the intervention (FMC) or control (delayed FMC) condition. Families assigned to the intervention condition will be asked to complete the FMC within 2 weeks of randomization and will be sent a second survey one week after completion. Participants in the control condition will complete a condition-specific subset of these questions three weeks after baseline. Participants in both conditions will complete a follow-up survey two months after their second survey.

The primary outcomes will be measured at the first follow-up period and will be related to screen media planning and decision making. Two-month follow-up surveys will explore intervention impact on screen media practices.

Prior to the clinical trial portion of the study, the study team conducted interviews/focus groups, participatory design sessions, and usability testing sessions with a diverse group of families to refine the concept for the intervention and to iteratively develop the intervention itself. Changes in the behavioral targets and components of the intervention and outcomes for the evaluation (relative to the original grant proposal) were driven by family-expressed needs and priorities.

Study Type

Interventional

Enrollment (Estimated)

300

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

Study Locations

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

11 years and older (Child, Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Children between the ages of 11 and 17
  • Parent/guardian of a child between the ages of 11 and 17
  • English speaking

Exclusion Criteria:

  • Parent/guardian or child does not want to participate (i.e., dyads only)
  • Non-English speaking

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: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Delayed FMC
Families assigned to the control condition will receive the FMC after study completion.
Experimental: FMC
Families randomized to the intervention condition will receive the FMC after they complete the baseline survey.
An interactive, web-based tool to support within-family media use planning will be developed and shared with families.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Decision Satisfaction
Time Frame: Baseline, 3 weeks post-baseline
Perceived Effective Decision Scale: a 4-item measure that assesses parent and teen satisfaction with their family media plan. Responses are measured on a 5-point Likert scale, with higher scores indicating a stronger perception of decision effectiveness.
Baseline, 3 weeks post-baseline
Decision Uncertainty
Time Frame: Baseline, 3 weeks post-baseline
Decision Uncertainty Scale: a 3-item scale adapted for the intervention and nature of decision designed to measure parent and teen perceptions of uncertainty when making decisions. The items evaluate factors contributing to uncertainty, including difficulty, lack of clarity, and indecision. Responses are recorded on a 5-point Likert scale. Higher scores indicate greater levels of perceived uncertainty, with the third item reverse-scored.
Baseline, 3 weeks post-baseline
Change in Family Media Planning and Plan Engagement
Time Frame: Baseline, 3 weeks post-baseline
Family Media Planning and Engagement Scale. This scale includes two components, each with 3 items: elements included in plan and engagement with plan. Higher scores indicate more screen media-related elements included in plan and greater teen engagement with plan.
Baseline, 3 weeks post-baseline
Teen Involvement in Plan
Time Frame: Baseline, 3 weeks post-baseline
This single-item assesses the degree of involvement teens perceive they had in creating the plan. Response options range from full individual control to full parent parental control, with options capturing varying levels of shared-decision making
Baseline, 3 weeks post-baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Screen Media Conflict
Time Frame: Baseline, 3 weeks post-baseline
3 items from the 2003 PEW Research Center Survey about how often parents and teens have argued in the past 2 weeks about three dimensions of teen screen media use.
Baseline, 3 weeks post-baseline
Screen-Related Parenting Style
Time Frame: Baseline, 3 weeks post-baseline
Perceived Parental Media Mediation Scale: a 15-item measure adapted for the main types of digital media use addressed in the intervention that assess teen perceptions of restrictive and active parental mediation. Responses are recorded on a 5-point Likert scale; responses to items are added together to create a total score, with higher scores indicating a greater perception of parental media mediation.
Baseline, 3 weeks post-baseline
Acceptability of FMC
Time Frame: 1 week post-intervention / 3 weeks post-baseline
Acceptability of Intervention Measure: a 4 item 4 point Likert scale with higher score indicating a higher level of acceptability
1 week post-intervention / 3 weeks post-baseline

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Amount of Use
Time Frame: Baseline, 3 weeks post-baseline
Parent and teen self-report of screen media use during a typical weekday and weekend for something other than school or work. Response options range from "I did not use screen media" to "6 or more hours".
Baseline, 3 weeks post-baseline
Social Media Addiction
Time Frame: Baseline, 3 weeks post-baseline
Bergen Social Media Addiction Scale: a 6-item measure to assess teen-reported dependence on social media. Each of the 6 items are rated on a 5-point Likert scale, with higher scores indicating a greater risk of social media addiction.
Baseline, 3 weeks post-baseline
Change in Problematic Media use
Time Frame: Baseline, 3 weeks post-baseline
Problematic Media Use Measure - Short Form: a 9-item scale which measures elements of addictive media use among children, including preoccupation, withdrawal, and unsuccessful attempts to control use by parents. Responses are recorded on a 5 point Likert scale with higher scores indicating more problematic media use.
Baseline, 3 weeks post-baseline
Parent Distracted Media Use
Time Frame: Baseline, 3 weeks post-baseline
Parent self-report and teen report of parent behavior. A single item question that measures how frequently parents are perceived as being distracted by their smartphones during conversations with their children. It is assessed using a question adapted from a PEW Center questionnaire, asked to both parents and teens. Response options include: often, sometimes, rarely, never distracted, or I/my parent does not have a smartphone.
Baseline, 3 weeks post-baseline
Emotional Health
Time Frame: Baseline, 3 weeks post-baseline
PedsQL Emotional Health subscale: A 5-item measure that assess emotional health in adolescents, focusing on the frequency of emotions such as sadness, anger, worry, or difficulty sleeping. ) Responses are recorded on a 5-point Likert scale (1=not at all to 5=very much), with higher scores reflecting higher levels of emotional well-being.
Baseline, 3 weeks post-baseline

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)

July 10, 2022

Primary Completion (Estimated)

August 1, 2026

Study Completion (Estimated)

August 1, 2026

Study Registration Dates

First Submitted

February 1, 2023

First Submitted That Met QC Criteria

February 1, 2023

First Posted (Actual)

February 10, 2023

Study Record Updates

Last Update Posted (Actual)

April 27, 2026

Last Update Submitted That Met QC Criteria

April 22, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 5R21HD107230 (U.S. NIH Grant/Contract)

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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