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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04101799
Other study ID # 2019-04227
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 21, 2019
Est. completion date June 30, 2020

Study information

Verified date September 2020
Source Karolinska Institutet
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Evaluation of the effects of the parental support intervention "For our children's sake" on positive parenting outcomes when conducted with incarcerated parents in prisons in Sweden.


Description:

Children of incarcerated parents comprise a greatly disadvantaged group in society with elevated risk of ill-health, behavioural problems, and own delinquency and unemployment later in life. Positive parenting comprise an important factor for children's positive and healthy development. Incarcerated parents may have difficulties to engage in positive parenting due to disadvantaged situations affecting parenting negatively such as drug addiction, poverty, or lack of experience of positive parenting in their own childhood. Previous research has suggested that interventions to prevent the intergenerational effect of criminality should be targeting family factors where positive parenting has been emphasised. Internationally developed parenting interventions for incarcerated parents suggest an impact on parenting outcomes such as positive parent-child interaction, parenting knowledge, empathy, parent stress, increased child contact and active parenting, However, the majority of the programmes evaluated to date have been conducted in the US, with a prison and probation context with limited generalisability to the Swedish system. In Sweden, the parenting programme for incarcerated parents, "For our children's' sake" (FOCS) was developed in 2012-2014 with the aim to support positive parenting for the child's healthy development and is currently delivered in Swedish prisons. The aim of this project is to evaluate the effects of the FOCS parenting programme on parenting outcomes through a controlled trial with a parallel implementation process evaluation.


Recruitment information / eligibility

Status Completed
Enrollment 91
Est. completion date June 30, 2020
Est. primary completion date June 30, 2020
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Serving a sentence at any of the included prisons

- Having at least one child in the ages between 0-18 years. Parents of children aged 0-2 and 13-18 years will not be included in the primary outcome measure, as the measure is not developed for these age groups. These parents will be included in the mediator measurements.

- Are in contact with their child/children in any form. If not, these parents are included in the mediator measurements, as the primary outcome: relationship quality, is not applicable.

- Having the legal right to contact the child

- Not committed either a crime against the child or any violent crime against the other parent

Exclusion Criteria:

- Not fulfilling inclusion criteria

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
For Our Children's Sake
Parental support with the aim to support positive parenting and promote healthy child development. Conducted in group-format with weekly 2.hour sessions conducted by trained group leaders according to a programme manual.
Other:
Active control
Participating in everyday activities that may include parenting activities in the control prisons

Locations

Country Name City State
Sweden Karolinska Institutet Stockholm

Sponsors (2)

Lead Sponsor Collaborator
Karolinska Institutet The Solstickan Foundation, The Sven Jerring Foundation

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Other 14 item parenting attitude from the The Adult-Adolescent Parenting Inventory (AAPI-2) Intermediate outcome/mediator self-reported on a 5-point scale ('complete agree' to 'completely disagree') Change in mean score of items between baseline (pre-intervention) and end of intervention, after 10 weeks. Measurements will also be conducted at mid-intervention to investigate mediated effects, and a 3-month post intervention follow-up.
Other 6 items parental self-efficacy scale Intermediate outcome/mediator self-reported on a 5-point scale ('complete agree' to 'completely disagree') Change in mean score of items between baseline (pre-intervention) and end of intervention, after 10 weeks. Measurements will also be conducted at mid-intervention to investigate mediated effects, and a 3-month post intervention follow-up.
Primary 7-items sub-scale Closeness in the Child Parent Relationship Scale Parent-reported quality in relationship between parent and child on a 5-point scale ('complete agree' to 'completely disagree') Positive change in mean score of all 7 items between baseline (pre-intervention) and end of intervention, after 10 weeks. Measurements will also be conducted at mid-intervention to investigate mediated effects, and a 3-month post intervention follow-up.
Secondary Contact frequency and type between parent and child Parent-reported frequency (weekly, monthly, less, no contact) and type (letter, telephone, visit/permission, other Change in mean score of items between baseline (pre-intervention) and end of intervention, after 10 weeks. Measurements will also be conducted at a 3-month post intervention follow-up.
Secondary Eight items chosen from the sub-scale antisocial intent in the Measures of Criminal Attitudes and Associates scale Parental attitude to criminality self-reported on a 5-point scale ('complete agree' to 'completely disagree') Change in mean score of items between baseline (pre-intervention) and end of intervention, after 10 weeks. Measurements will also be conducted at a 3-month post intervention follow-up.
Secondary Parent interest in other treatment programmes in prison One item self-reported on an 11-point scale (0 no interest, 10 very high interest) Change in item score between baseline (pre-intervention) and end of intervention, after 10 weeks. Measurements will also be conducted at a 3-month post intervention follow-up.
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