An evaluation of a wraparound intervention for families whose children are at risk of abuse and/or neglect

Not Applicable

Completed

• Conditions: Child abuse and neglect; Mental and Behavioural Disorders

• Registration Number: ISRCTN13644600
• Lead Sponsor: Maynooth University

Brief Summary

2018 protocol in https://www.ncbi.nlm.nih.gov/pubmed/32002506 (added 03/02/2020)

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2015-06-03
• Study Completion: 2018-12-10
• Last Update Posted: 22 February 2021

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 41

Inclusion Criteria

1. Participants are parents/caregivers (both genders) of children aged 3-10 years (both genders) where:
1.1. The child has been identified by a child welfare professional within a collaborating agency (e.g. social work team) as being at risk of abuse or neglect; or
1.2. Where it is known by the social work team that a level of child maltreatment has occurred, but the child is still living within the home (i.e. not placed in state care)

The child’s level of risk will be judged according to Levels 2 to 4 in line with the guidance contained in the document entitled ‘Thresholds for referral to Tusla Social Work services’. This document is based on the Hardiker model.

2. Parents/caregivers must be judged by the social work team to be stable in terms of substance use, domestic violence or mental illness so that they have the capacity to engage for the duration of the intervention
3. In cases where families, and particularly high risk families, are on mandatory child protection plans and are allocated to the control group, they must be provided with interim support from their allocated social care leader/key worker until they receive the wraparound intervention. This support may involve usual services such as individual therapy, as well as referral to services that are not part of the ‘core’ wraparound intervention
4. Parents/families must be willing and able to attend the services offered
5. Parents/families must agree to participate in the research

Exclusion Criteria

1. Families who display unstable substance use or mental illness will be excluded as will those who are considered to be unstable due to domestic violence issues
2. Families who have had prior exposure to an evidence-based parenting programme will be excluded

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<br> 1. Improvement in child wellbeing and behaviour - measured by the Strengths and Difficulties questionnaire (SDQ), completed by parent (and child, where appropriate) at baseline, 6-, 12- and 18-month follow up<br> 2. Reduction in incidences of child abuse and neglect - Conflict Tactics Scale Parent Child, completed by parent at baseline, 6-, 12- and 18-month follow up<br> 3. Reduction in child abuse potential - measured by the Brief Child Abuse Potential Inventory, competed by parent/caregiver at baseline, 6-, 12- and 18-month follow up<br>

Secondary Outcome Measures

Name	Time	Method
<br> 1. Improvement in parental mental health - measured by the Depression, Anxiety and Stress scale (DASS) and the Parenting Stress Index, both completed by parent at baseline, 6-, 12- and 18-month follow up<br> 2. Improvement in parental alcohol and drug use - measured by the CAGE and Drug Abuse Screening Test (DAST-10) questionnaires, both completed by parent at baseline, 6-, 12- and 18-month follow up<br> 3. Improvement in the relationship between parent and children - measured by the Parenting Stress Index (PSI) and the HOME observation. The PSI is completed by parents. The HOME is conducted by researchers observing parent-child interaction. Both measures are administered at baseline, 6-, 12- and 18-month follow up<br> 4. Improvement in parenting competencies - measured by the HOME observation, completed by researchers observing parent-child interaction at 6-, 12-, and 18-month follow up<br>