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Active Not RecruitingNCT06099457

SIBTime Phase II: Web Application for Typically Developing Siblings

SIBTime: Media-enhanced Technology for Promoting the Behavioral Health and Family Relationships of Typically Developing Young Siblings

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
160 (estimated)
Sponsor
Oregon Research Behavioral Intervention Strategies, Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Most of the over 32.7 million people in the U.S. who have special health, developmental, and mental health concerns have typically developing (TD) brothers and sisters who share high levels of involvement in their sibling's lives. Disability and health agencies lack effective tools to support the information and support needs of TD siblings and their families, in particular for ethnic minority and rural families. The aims of this proposal are to complete development and evaluation of the dual language SIBTime app, designed to build parents' and children's knowledge, skills, and engaging family routines to nurture TD siblings' (ages 3-6) social-emotional health and well-being.

Detailed description

An 8-week RCT will be conducted to evaluate the full-scale SIBTime program in a sufficiently powered randomized controlled trial evaluation (sample size = 160 parent/child dyads). SIBTime will be assessed in terms of its relevance, acceptability, cultural appropriateness, and efficacy. Participants will complete measures pre- and post- intervention selected to detect changes in parenting stress and adjustment, parent-child relationship, parents' self-efficacy and frequency of engagement in the targeted parenting strategies, and TD sibling behavior and adjustment. Information will also be collected on family demographics, consumer satisfaction, usability ratings, usage metrics, and recommendations for modifications to the program.

Conditions

Interventions

TypeNameDescription
BEHAVIORALSIB-Time web-application toolParent-child dyads will use the SIBTime app in an 8-week intervention to test its relevance, acceptability, cultural appropriateness, and potential for efficacy.

Timeline

Start date
2023-10-27
Primary completion
2026-02-02
Completion
2026-04-08
First posted
2023-10-25
Last updated
2026-03-09

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06099457. Inclusion in this directory is not an endorsement.