Skip to main content
Clinical Trials/NCT01389726
NCT01389726
Completed
Phase 1

Comparing Interventions To Improve The Well-Being Of Custodial Grandfamilies

Kent State University4 sites in 1 country343 target enrollmentJanuary 2012

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Custodial Grandparents
Sponsor
Kent State University
Enrollment
343
Locations
4
Primary Endpoint
Change in Parenting Quality after intervention up to two years
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

This study is a multi-site, four-year long clinical trial study in which several mental health interventions will be delivered to custodial grandmothers and then compared. The study will examine effects on the mental health of these grandmothers and the grandchildren they provide full-time care to in complete absence of the grandchild's birth parents. Grandparents from diverse racial, ethnic, and socio-economic backgrounds will be recruited to test for cultural differences in response to these interventions. This study is important because there is growing evidence that custodial grandchildren are at-risk for psychological difficulties due to neglect and abuse by birth parents, challenges to parenting faced by custodial grandparents, and limited access to needed services. This study is funded by the National Institute of Nursing Research, a division of the National Institutes of Health, and it is anticipated that more than 500 custodial grandfamilies in four sites across the United States will partake.

Detailed Description

Although prior studies reveal that custodial grandmothers (CGM) and grandchildren (CGC) face high risk for psychological difficulties, virtually no rigorous studies of psychosocial interventions based on solid conceptual frameworks have been conducted with these vulnerable families. In view of preliminary findings that disrupted parenting mediates the relationship between CGM's psychological distress in the caregiver role and CGC's emotional and behavioral problems, this project involves a randomized clinical trial (RCT) of the comparative feasibility and efficacy of two evidenced-based psychoeducational interventions widely used with other caregiver populations. Grandmothers (N = 504) of CGC (age 5 - 12) will be randomly assigned to one of three conditions: Behavioral Parent Training (BPT; derived from Project KEEP for foster parents; Cognitive Behavioral Therapy (CBT; derived from Coping with Caregiving for caregivers of frail elders); Minimal Support Condition (to control for non-specific treatment factors). The proposed universal interventions include prevention and remediation objectives and involve a group format approach with mental health professionals and grandparent peers serving as co-leaders. The RCT will occur in multiple locations across the US to ensure that findings generalize beyond a single area and that equal numbers of Black (n = 168), Hispanic (n = 168), and White (n = 168) families participate. Prior to the RCT, focus groups will be held separately with CGMs of each race (n = 10 apiece) and experienced practitioners (n = 10) with the aim of assessing the perceived importance and acceptability of recruitment methods, treatment goals, and procedures, including possible differences by race/ethnicity. Multiple-informant and multiple-method assessments during the RCT at pretest, posttest and 6, 12, 18, and 24 month follow-ups will include indicators of CGM psychological distress (anxiety, depression); CGC adjustment (internalizing and externalizing problems); and disrupted parenting (use of ineffective discipline and low nurturance). Based on the conceptual framework of the prominent Family Stress Model, multi-group structural equation modeling analyses will be used to achieve four aims: (a) To compare the short and long-term effectiveness of CBT and BPT; (b) to examine longitudinally the dynamic linkages between CGM parenting practices, CGM' psychological distress, and CGC adjustment as modified by BPT and CBT; (c) to determine if key moderating variables (race/ethnicity, CGC, initial psychological difficulties in CGC and CGM influence RCT outcomes; and (d) to examine key factors related to acceptability and adherence to the proposed interventions. The findings will inform future clinical practice with custodial grandfamilies by identifying which of the proposed interventions are most effective and most acceptable among specific sub-groups (e.g., race/ethnicity; initial risk) and by unraveling the specific antecedent-consequent relations among CGM distress, dysfunctional parenting, and CGC adjustment.

Registry
clinicaltrials.gov
Start Date
January 2012
End Date
October 2014
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Grandmother raising grandchildren
  • No biological resides in grandmother's home
  • At least one grandchild between ages 4 and 12
  • Grandchild has lived with grandmother for minimum of 3 months
  • Grandchild is expected to stay with grandmother

Exclusion Criteria

  • Biological parent is directly involved in raising child
  • Grandmother is unable to leave the home to attend weekly meetings
  • Grandmother is unable to speak English
  • Grandmother is unable to answer simple questions

Outcomes

Primary Outcomes

Change in Parenting Quality after intervention up to two years

Time Frame: post-test (2 to 6 weeks following intervention), 6 mos, 12 mos, 18 mos, 2 years

Parenting quality will be measured in terms of the degree to which grandparents employ positive discipline strategies and engage in warm or nurturing parenting styles. Measured both using self-report and observer ratings.

Secondary Outcomes

  • Change in GM Psychological Distress after intervention up to two years(post-test (2 to 6 weeks following intervention), 6mos, 12 mos, 18 mos, 24 mos)
  • Change in Grandchild Internalizing and Externalizing Symptoms after intervention up to two years(post-test (2 to 6 weeks following intervention), 6 mos, 12 mos, 18 mos, 24 mos)
  • Intervention efficacy(2 to 6 weeks following intervention)

Study Sites (4)

Loading locations...

Similar Trials