Viewing Study NCT06099262



Ignite Creation Date: 2024-05-06 @ 7:40 PM
Last Modification Date: 2024-10-26 @ 3:11 PM
Study NCT ID: NCT06099262
Status: RECRUITING
Last Update Posted: 2023-10-25
First Post: 2023-09-26

Brief Title: GenPMTO Evaluation
Sponsor: The Behavioural Insights Team
Organization: The Behavioural Insights Team

Study Overview

Official Title: GenPMTO - Adaptation and Feasibility Study
Status: RECRUITING
Status Verified Date: 2023-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This project is a multi-stage evaluation of GenPMTO Generation Parent Management Training - Oregon Model GenPMTO is a parenting programme which involves trained practitioners using active teaching approaches such as group problem-solving role-play and video modelling to support caregivers in using positive parenting strategies at home The programme is designed to improve parenting practices as well as a range of outcomes for young people including improving academic performance reducing school exclusions and reducing offending and criminal behaviour The version of the programme investigated in this project is delivered to groups of parents
Detailed Description: This project represents the first attempt to deliver and evaluate GenPMTO in the UK To do so the Ending Youth Violence Lab at the Behavioural Insights Team is conducting a multi-stage evaluation involving delivering the intervention across three London boroughs with a focus on caregivers of 8-14-year-old children and young people CYPs who are identified to have risk factors associated with involvement in violence

To design this project the Lab has collaborated with two partners The first is ISII Implementation Sciences International Inc a research-based non-profit organisation based in the USA which implements the GenPMTO programme in partnership with the programme developers ISII also trains community practitioners in its use across the world The second partner is Barnardos the UKs largest childrens charity and the delivery partner for the project

This entry refers to the first 2 stages of the project which will run concurrently

Stage 1 - Adaptation and training

The purpose of this Stage is to prepare for initial delivery and the feasibility testing of delivery by making any adaptations that may be necessary for the UK context and beginning practitioner training
The research objectives of this Stage firstly focus on identifying whether the programme may require adaptations to fit into the UK context and identifying and justifying appropriate adaptations Secondly the investigators want to identify whether sufficient numbers of practitioners can be recruited and trained within the budget of the project and to identify the optimal approach to recruitment and training of future practitioner cohorts to allow delivery at a larger scale

Stage 2 - Feasibility study

The purpose of this Stage is to understand the feasibility of delivering GenPMTO to the caregivers of children who have been identified as being at risk of violence through testing recruitment retention fidelity etc The investigators will also conduct further adaptation to the programme as necessary responding to what we learn from practitioners and caregivers who have experienced the programme for the first time

The specific research objectives here focus on

Feasibility - Can Barnardos recruit and retain caregivers of children who meet inclusion criteria and are at risk of youth violence and deliver the programme withfidelity
Acceptability - Is the GenPMTO programme seen as acceptable and valuable by caregivers and practitioners in a UK context
Evaluability - Firstly is there sufficient demand and capacity to deliver GenPMTO at a scale required for a randomised control trial Secondly is it feasible to collect outcome data from participants which would support robust outcome data collection procedures during a pilot andor efficacy trial

This will involve delivering the programme in 3 London boroughs and collecting a range of survey data and conducting qualitative interviews with caregivers and with practitioners to explore the above questions The investigators will collect pre- and post-programme outcome data using a range of self-report measures to explore the potential for future robust evaluation rather than to assess programme impact

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None