An evaluation of the Incredible Years Parent Programme in Birmingham: support for parents of 3 and 4 year old children displaying problem behaviour
| ISRCTN | ISRCTN48762440 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN48762440 |
| Protocol serial number | L680 TA-01631-01 RVPOG AOO |
| Sponsor | Birmingham County Council (UK) |
| Funder | Birmingham County Council (UK) (ref: L680 TA-01631-01 RVPOG AOO) |
- Submission date
- 08/10/2009
- Registration date
- 15/12/2009
- Last edited
- 18/07/2016
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Mental and Behavioural Disorders
Plain English summary of protocol
Not provided at time of registration
Contact information
Scientific
The Social Research Unit
Lower Hood Barn
Dartington
TQ9 6AB
United Kingdom
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Single centre randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| Study type | Participant information sheet |
| Scientific title | A randomised controlled trial of the Incredible Years Parent Programme with parents of children at risk of developing conduct disorder in nine areas across Birmingham City |
| Study objectives | 1. There will be an improvement in parenting competencies following parent training 2. Children whose parents received parent training will show reduced problem behaviour and hyperactivity, and improved social competence 3. The programme will offer value for money and net benefit to the Council |
| Ethics approval(s) | Warren House Group Ethics Committee, 05/03/2009, ref: WHG 2009-1 |
| Health condition(s) or problem(s) studied | Conduct disorder (CD) |
| Intervention | The 12-week Incredible Years BASIC Parent Programme will be delivered as an early intervention to parents of children already displaying problematic behaviour in order to reduce the likelihood of children developing conduct disorder. The waiting list control group will be offered the intervention after the final follow up. The total duration of follow-up will be 12 months after baseline for both arms of trial. |
| Intervention type | Other |
| Primary outcome measure(s) |
Administered at baseline, and the 6- and 12-month follow-ups: |
| Key secondary outcome measure(s) |
Parent report at baseline, 6- and 12-month follow-ups: |
| Completion date | 30/03/2011 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Child |
| Lower age limit | 3 Years |
| Upper age limit | 4 Years |
| Sex | All |
| Target sample size at registration | 162 |
| Key inclusion criteria | 1. Live within one of the designated nine Children Centre catchment areas 2. Child aged 3 - 4 years, either sex 3. Scoring above the clinical cut-off of 17 for total difficulties on the Strengths and Difficulties Questionnaire (SDQ) |
| Key exclusion criteria | 1. Child aged below 3 or above 4 years 2. Scored below the clinical cut off of 17 on the SDQ |
| Date of first enrolment | 01/11/2009 |
| Date of final enrolment | 30/03/2011 |
Locations
Countries of recruitment
- United Kingdom
- England
Study participating centre
TQ9 6AB
United Kingdom
Results and Publications
| Individual participant data (IPD) Intention to share | No |
|---|---|
| IPD sharing plan summary | Not provided at time of registration |
| IPD sharing plan |
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|---|---|---|---|---|
| Participant information sheet | Participant information sheet | 11/11/2025 | 11/11/2025 | No | Yes |
| Study website | Study website | 11/11/2025 | 11/11/2025 | No | Yes |
Editorial Notes
18/07/2016: No publications found, verifying study status with principal investigator.