Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05405972
Other study ID # STUDY00000382
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 15, 2022
Est. completion date November 30, 2023

Study information

Verified date May 2024
Source University of Arizona
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate a behavioral intervention with foster families.


Description:

Study Aims: This study aims to investigate a technology-delivered family (sibling inclusive) intervention. Focus is on increasing family hardiness and preparation to care for children with disabilities and special needs in foster care. Three aims include: (1) establish the feasibility of the technology-based, family-centered intervention (2) explore in a preliminary manner the effects of the intervention on stress and relational quality outcomes among family member participants, and (3) an exploratory aim to determine feasibility and preliminary efficacy of the intervention on diurnal salivary cortisol levels within the foster family population. Methods: This study employs a randomized control trial design of a behavioral intervention with both a control and experimental group. The intervention tested was created in partnership and adapted from the Connected Family Series (CFS) by psychologists at the Karyn Purvis Institute of Childhood Development and is called the Connected Family Series - For Foster Families (CFS-FF). Adaptation was needed as the original intervention was geared toward adoptive families and excluded foster families. The CFS-FF also needed content specific to fostering children with special needs. Stress and relational quality outcomes among members will be measured using the concepts of family hardiness, preparedness, and relationship development through a self-report questionnaire which include the Family Hardiness Index (FHI), the Integrating Foster Children (IFC) subscale from the Casey Foster Applicant Inventory (CFAI), and the Sibling Inventory of Behavior (SIB), respectively. Participation in the study spanned three to four months; one month for recruitment and collection of baseline data, one month for the intervention, and one-month post-intervention data collection. Exploratory aim 3 will be achieved by an objective indicator of stress-related biology, saliva diurnal cortisol rhythm, before and after completion of the intervention.


Recruitment information / eligibility

Status Completed
Enrollment 95
Est. completion date November 30, 2023
Est. primary completion date August 30, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 7 Years to 85 Years
Eligibility Inclusion Criteria: 1. licensed foster families 2. must have at least one permanent child (biological or adopted) living in the home before the foster or newly adopted child entered the home 3. at least one foster or foster-to-adopt child placed in the home 4. all participants other than the foster or foster-to-adopt child must be proficient in English Exclusion Criteria: 1. Non-English speaking 2. No permanent sibling between the ages of 7 at 17 3. No current foster placement living in the home 4. Designated as a group home 5. Greater than six children living in the home

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
The Connected Family Series - For Foster Families
A 4-week program involving videos and activities for both the parent and child in the home.

Locations

Country Name City State
United States University of Arizona Tucson Arizona

Sponsors (1)

Lead Sponsor Collaborator
University of Arizona

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Family Hardiness Index Psychometrically validated self-report tool for family functioning. Unabbreviated scale title: Family Hardiness Index Min Value: 0 Max Value: 60 Higher Score means better/improvement in hardiness After intervention, up to 3 months
Other Sibling Inventory of Behavior Psychometrically validated self-report tool for sibling relationships. Unabbreviated scale title: Sibling Inventory of Behavior (Positive) Min Value: 15 Max Value: 75 Higher Score means there are more positive outcomes between the siblings
Unabbreviated scale title: Sibling Inventory of Behavior (Negative) Min Value: 17 Max Value: 85 Higher Score means there are more negative outcomes between the siblings
After intervention, up to 3 months
Primary Family Hardiness Index Psychometrically validated self-report tool for family functioning. Unabbreviated scale title: Family Hardiness Index Min Value: 0 Max Value: 60 Higher Score means better/improvement in hardiness Before intervention, up to 2 week
Secondary Sibling Inventory of Behavior Psychometrically validated self-report tool for sibling relationships. Unabbreviated scale title: Sibling Inventory of Behavior (Positive) Min Value: 15 Max Value: 75 Higher Score means there are more positive outcomes between the siblings
Unabbreviated scale title: Sibling Inventory of Behavior (Negative) Min Value: 17 Max Value: 85 Higher Score means there are more negative outcomes between the siblings
Before intervention, up to 2 weeks
See also
  Status Clinical Trial Phase
Recruiting NCT05987761 - PRT for Adolescents With High Functioning Autism N/A
Completed NCT03617952 - P3 Ghana Cookstove Study N/A
Completed NCT04382560 - Coping Strategies and Responsiveness to a Brief Online Intervention During COVID-19 Pandemic N/A
Recruiting NCT04115124 - Using Ethnographic Participatory Action Research to Decrease the Incidence of Female Genital Mutilation in Nigeria N/A
Completed NCT03974282 - Brain Function and Decision-Making N/A
Completed NCT03949569 - The Effects of Therapy Dogs on Child Biology and Behavior N/A
Completed NCT04269824 - The Norms and Networks Sanitation Study in India in Tamil Nadu, India N/A
Completed NCT04458077 - Discover Learning - Social, Emotional and Identity Learning for Very Young Adolescents N/A
Completed NCT03642197 - Feasibility and Preliminary Efficacy of Support Figure Attendance at Bariatric Patients' Clinical Visits N/A
Recruiting NCT06086600 - Instrument Assisted Soft Tissue Mobilization Versus Dynamic Oscillatory Stretch Technique in Females Wearing High Heels N/A