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Evaluation of an internet-based weight loss intervention

Evaluation of an internet-based weight loss intervention: a randomised trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN48086713
Enrollment
120
Registered
2012-10-26
Start date
2012-10-22
Completion date
Unknown
Last updated
2018-04-30

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

Participants randomised to the internet based weight loss intervention will meet with a dietitian once face to face. After the initial meeting participants will only receive guidance via a website thr

Sponsors

County Durham and Darlington NHS Foundation Trust (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Two target groups: 1.Women who have had a baby (from 3 months up to 2 years after childbirth) and, who currently have a body mass index (BMI) >˜30 and ˜30 and ˜30 and <40 kg/m2. 3. Participants must have access to the internet (this can be in any location [home, office, public location] or on any device [desktop computer, laptop or mobile phone])

Exclusion criteria

Exclusion criteria: 1. Patients over BMI 40 kg/m2. When a patient reaches a BMI 40kg/m2 lifestyle modification may no longer be appropriate and bariatric surgery may be recommended (National Institute for Health and Clinical Excellence, 2006), making it unsuitable for them to take part in the study. 2. Patients unable to access the internet 3. Patients unable to give written informed consent in English. These patients would be excluded as they would be unable to randomise to the internet intervention which is only available in English. The resources are not available to use a translator in this study or produce the web-based resources in other languages. 4. Patients identified by their GP as having a contraindication making the weight loss intervention inappropriate to recommend 5. Patients who are currently pregnant will be excluded from the study

Design outcomes

Primary

MeasureTime frame
Participant Involvement (recruitment, attrition, retention) at baseline, 3 months and 12 months

Secondary

MeasureTime frame
1. 24 hour diet recall at baseline, 3 months and 12 months 2. Acceptability Interviews between 6 and 12 months 3. Anthropometric measures (weight, body fat percentage, waist circumference and BMI) at baseline, 3 months and 12 months 4. Predictors of behaviour change at baseline, 3 months and 12 months 5. Quality of life questionnaire at baseline, 3 months and 12 months

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 26, 2026