Skip to content

Service-review and feasibility trial in paediatric weight management

A feasibility study exploring patient perceptions of a paediatric weight-management programme, and the suitability of introducing a response inhibition training app to the treatment programme

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN11102100
Enrollment
80
Registered
2018-12-10
Start date
2018-12-12
Completion date
Unknown
Last updated
2021-10-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Childhood obesity Nutritional, Metabolic, Endocrine Childhood obesity

Interventions

There are two strands to this research project. Firstly, a qualitative service review that will be based on interviews with the service users of the COCO clinic and their families. Secondly, a feasibi

Sponsors

University of Bristol
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Attendance at a weight management course or program due to excessive weight 2. Participant gives assent to participate 3. Participants parent/guardian gives consent to their child’s participation (if under 16) Clinic staff will also be recruited for participation in the study to determine feasibility and acceptability from their perspective. The inclusion criteria for staff are: 1. Employment in the obesity or weight management clinic 2. Involvement in the treatment of those using the FoodT app

Exclusion criteria

Exclusion criteria: 1. Problems with eyesight that cannot be corrected with glasses and prevent the participant from seeing the food images on the phone screen 2. The participant does not speak English or understand written English 3. Concurrent participation in a trial investigating a weight-loss intervention

Design outcomes

Primary

MeasureTime frame
Feasibility measured via: 1. Qualitative interviews and/or questionnaires with staff, patients and their families at the end of the 12-week trial period 2. Recruitment rates 3. Adherence measured through in-app data collection that reports on frequency of play

Secondary

MeasureTime frame
Benefit measured by: 1. Qualitative feedback via interviews and/or questionnaires at the end of the trial period 2. Self-reported consumption frequency of common snack foods (in app & online survey) at the start and end of trial (week 0 and week 12) 3. Food liking measured by a Visual Analogue Scale (VAS) (online survey) at the start and end of trial (week 0 and week 12) 4. Food preference measured using a forced-choice food task (online survey) at the start and end of trial (week 0 and week 12)

Countries

England, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026