Evaluation of a Family Strengthening Program Evaluation in Sierra Leone to Prevent Family Separation

Sponsor
Boston College (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05632237
Collaborator
Christian Alliance for Orphans (Other), Helping Children Worldwide (Other), Child Reintegration Centre (Other)
226
1
2
4.5
50.6

Study Details

Study Description

Brief Summary

In Sierra Leone, poverty and challenges with family functioning can lead to family separation, and children may go to live on the street or enter residential care institutions/orphanages. Helping Children Worldwide (HCW), a non-profit organization with over 20 years of experience in Sierra Leone, has developed a two-part Family Strengthening Program delivered by their program partners in Sierra Leone, the Child Reintegration Centre, to improve families financial literacy and attachment between caregivers and children, with the ultimate goal of preventing family separation. The hypothesis of this study is that the Family Strengthening Program program is effective at (1) changing parenting behaviors, (2) improving emotional regulation, (3) improving caregiver-child attachment, and (4) improving financial literacy in dyads consisting of children ages 9-13 and their caregivers.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Family strengthening program
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
226 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Masking Description:
During baseline data collection, participants were not yet assigned to arms, so all parties were masked.
Primary Purpose:
Prevention
Official Title:
Evaluation of a Family Strengthening Program Evaluation in Sierra Leone to Prevent Family Separation
Actual Study Start Date :
Oct 16, 2022
Anticipated Primary Completion Date :
Mar 1, 2023
Anticipated Study Completion Date :
Mar 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Family strengthening program

Behavioral: Family strengthening program
Phase I: 2-day Family Strengthening Workshop. The specific topics included in the workshop include: emotions, Body Progressive Muscle Relaxation, body stretch, self care, apologizing, routines to promote attachment, teamwork, saving, delayed gratification, anticipating unexpected expenses, identifying family strengths and values. Phase II: Case management with family strengthening curriculum. Curriculum is delivered over the course of four visits (about 3 months), some of which involve both caregiver and child while others are just for the caregiver. Topics included are using appropriate discipline, effective communication for family problem-solving, and home budgeting.

No Intervention: Care as usual

These participants have already been receiving case management from the Child Reintegration Centre prior to the study, and they will continue to receive care as usual, which is to receive normal case management visits without this added Family Strengthening Program component. Case management consists of a social work staff alternating between visiting children at home or at school each month to provide supervision, coaching, counseling, assessments, and identification of additional support needs.

Outcome Measures

Primary Outcome Measures

  1. Caregiver and child change in emotional regulation as measured by the Difficulties in Emotional Regulation (DERS) scale [Baseline: Up to 2 months before intervention; Endline: Up to 2 months after intervention]

  2. Change in child attachment as measured by the Inventory of Parent and Peer Attachment (IPPA) [Baseline: Up to 2 months before intervention; Endline: Up to 2 months after intervention]

  3. Change in caregiver- and child-reported use of punishment by caregiver [Baseline: Up to 2 months before intervention; Endline: Up to 2 months after intervention]

    Measures developed for this study tailored for context; e.g., flogging child with hand or cane, public shaming, withholding food

  4. Change in self-reported economic well-being [Baseline: Up to 2 months before intervention; Endline: Up to 2 months after intervention]

    Measures developed for this study tailored for context and intervention content; e.g., awareness of income/spending, saving and budgeting behaviors, ability to pay for unexpected expense

Secondary Outcome Measures

  1. Change in child- and caregiver-reported parenting behaviors by caregiver [Baseline: Up to 2 months before intervention; Endline: Up to 2 months after intervention]

    Measures developed for this study tailored for context and intervention content; e.g., asking child about their life, spending one-on-one time with child, physically showing affection, giving compliments/praise, using a routine, apologizing, providing emotional support

Eligibility Criteria

Criteria

Ages Eligible for Study:
9 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion criteria:
  1. Dyads must consist of a principal child (the one whose situation initiated their involvement with the Child Reintegration Centre) and their primary caregiver (as defined by the Child Reintegration Centre as the person in the family primarily responsible for the health and wellbeing of the principal child and is noted as such in their case file)

  2. Primary child is ages 9-13

  3. Dyad is actively participating in Child Reintegration Centre services (i.e., child must have been seen by the case manager in the last month)

  4. Dyad lives in the Bo area.

Exclusion criterion:

(1) Family has been assessed by the Child Reintegration Centre to be in active crisis, i.e., specific concerns about the child being at-risk or unsafe (suspicions of abuse or neglect).

Contacts and Locations

Locations

Site City State Country Postal Code
1 the Child Reintegration Centre Bo Sierra Leone

Sponsors and Collaborators

  • Boston College
  • Christian Alliance for Orphans
  • Helping Children Worldwide
  • Child Reintegration Centre

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sarah Neville, PhD, Boston College
ClinicalTrials.gov Identifier:
NCT05632237
Other Study ID Numbers:
  • cafo
First Posted:
Nov 30, 2022
Last Update Posted:
Jan 19, 2023
Last Verified:
Jan 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jan 19, 2023