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Group Receiving Intervention for Relationship or Family Issues
N/A
Waitlist Available
Led By Christine Platt, DNP/PhD
Research Sponsored by University of Arizona
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up after intervention, up to 3 months
Awards & highlights
Study Summary
The purpose of this study is to investigate a behavioral intervention with foster families.
Eligible Conditions
- Relationship or Family Issues
- Sibling Relations
- Social Behavior
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ after intervention, up to 3 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~after intervention, up to 3 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Other outcome measures
Family Hardiness Index
Sibling Inventory of Behavior
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Group Receiving InterventionExperimental Treatment1 Intervention
The intervention group receives a link each week connecting them to the videos for both parents and children as well as a communicating/connecting activity. The intervention is self-paced over a 4 week period.
The intervention was titled the Connected Family Series - For Foster Families (CFS-FF) (further referred to as the intervention) and was created/adapted in partnership from the Connected Family Series (CFS) by psychologists at the Karyn Purvis Institute of Childhood Development (KPICD). A letter of support from the KPICD is available in Appendix D. Adaptation was needed as the original intervention was geared toward adoptive families and excluded foster families. This process was done with the original creator (Dr. Jana Hunsley) with members of the research team and fostering community.
Group II: Control GroupActive Control1 Intervention
Families in the control group receive no video links during the 4 week period. Families assigned to the control do have the opportunity to participate in the intervention post-data collection and analysis and outside of the research protocol.
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Who is running the clinical trial?
University of ArizonaLead Sponsor
514 Previous Clinical Trials
148,464 Total Patients Enrolled
Christine Platt, DNP/PhDPrincipal InvestigatorUniversity of Arizona
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Who else is applying?
What state do they live in?
California
How old are they?
65+
What portion of applicants met pre-screening criteria?
Did not meet criteria
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