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Is it feasible and acceptable to deliver HELPclinic (Healthy Eating Lifestyle Programme by Clinicians) in the medical office (outpatient) setting?

Healthy Eating Lifestyle Programme by Clinicians: a feasibility randomised control pilot trial

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN10921803
Enrollment
40
Registered
2016-10-26
Start date
2010-10-17
Completion date
Unknown
Last updated
2020-02-24

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

Conditions

Obesity Nutritional, Metabolic, Endocrine Obesity

Interventions

All participants in this study undertake the HELPclinic intervention, a five-session individual lifestyle programme delivered at monthly intervals. The lifestyle intervention uses behavioural tools fr

Sponsors

University College London Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 12-18 years 2. Male and female 3. BMI between 98th centile and 45kg/m2

Exclusion criteria

Exclusion criteria: 1. Subjects with significant mental health problems or undergoing mental health treatment 2. Other chronic illness, monogenic obesity syndrome or use of medications known to promote obesity 3. Patients who have signs or symptoms which require them to have immediate investigations, e.g. diabetes 4. Participants with significant learning disability or lack of command of English sufficient to render them unable to participate effectively in the planned intervention. The great majority of eligible young people from black or minority ethnic groups in this population have good command of English. Given the importance of standardising the intervention, it will not be possible to use interpreters to enable parents with poor English to participate. We will ensure that the external validity of the study is maintained by allowing another relative with good English to participate 5. BMI>45 kg/m2 as they are unlikely to respond to lifestyle changes alone 6. Participants who have been involved in a weight management research program greater than 12 months previously will be eligible but those who are actively involved in a weight management program will be excluded

Design outcomes

Primary

MeasureTime frame
1. Feasibility - recruitment, attendance and attrition rates are continually monitored in order to test the ability to recruit and retain participants 2. Acceptability - qualitative interviews are performed with participants and clinicians after 6-12 months of study completion

Secondary

MeasureTime frame
Change in BMI over the course of the programme: height and weight are measured at each session and 1 month after completion of the programme

Countries

United Kingdom

Contacts

Public ContactBilly White
billy.white@ucl.ac.uk+44 (0)20 3447 9221

Outcome results

None listed

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