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Optimising a digitally delivered behavioural weight loss programme: study protocol for a factorial cluster randomised controlled trial.
Wren, Gina M; Koutoukidis, Dimitrios A; Scragg, Jadine; Preston, Grace; Hennessy, Marianne; Estephane, Daisy; Whitman, Michael; Jebb, Susan A.
Afiliación
  • Wren GM; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK. gina.wren@phc.ox.ac.uk.
  • Koutoukidis DA; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
  • Scragg J; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
  • Preston G; Second Nature, London, UK.
  • Hennessy M; Second Nature, London, UK.
  • Estephane D; Second Nature, London, UK.
  • Whitman M; Second Nature, London, UK.
  • Jebb SA; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
Trials ; 25(1): 477, 2024 Jul 13.
Article en En | MEDLINE | ID: mdl-39003481
ABSTRACT

BACKGROUND:

Digitally delivered weight loss programmes can provide a convenient, potentially cheaper, and scalable treatment option for people who may need to lose weight. However, outcomes are often inferior to in-person interventions in the long-term. This trial will use principles from the Multiphase Optimisation Strategy (MOST) framework to test whether it can enhance the effectiveness of a commercial digital behavioural weight loss programme. This trial aims to identify an optimised combination of four intervention components to enhance weight loss over a 24-week period. We will also explore which components contribute to improvements in participant retention and engagement with the programme.

METHODS:

Approximately 1400 adults with a BMI > 21 kg/m2 will be enrolled and randomised to one of 16 experimental conditions in a 24 factorial cluster design. The trial will test four intervention components an introductory video call with the health coach, drop-in webchat sessions with the health coach, goal setting statements, and food diary review and feedback. All participants will receive the core digital behavioural weight loss programme and up to four new intervention components. Participation in the trial will last for 24 weeks. The primary outcome will be weight change at 16 weeks. Other outcomes, measured at 4, 16, and 24 weeks, include programme drop-out and engagement (number of interactions with the three main app functions). Fidelity and acceptability will be assessed using data on component adherence and self-report questionnaires. Decision-making for the enhanced programme will be based on components that contribute to at least a minimal improvement in weight loss, defined as ≥ 0.75kg, alone or in combination with other components.

DISCUSSION:

The factorial design is an efficient way to test the efficacy of behavioural components alone, or in combination, to improve the effectiveness of digital weight loss programmes. This trial will test the implementation of the MOST framework in an industry setting, using routinely collected data, which may provide a better way to refine and evaluate these types of interventions in a model of continuous service improvement. TRIAL REGISTRATION Trial registration ISRCTN, ISRCTN14407868. Registered 5 January 2024, 10.1186/ISRCTN14407868.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Terapia Conductista / Pérdida de Peso / Ensayos Clínicos Controlados Aleatorios como Asunto / Programas de Reducción de Peso Límite: Adult / Female / Humans Idioma: En Revista: Trials Asunto de la revista: MEDICINA / TERAPEUTICA Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Terapia Conductista / Pérdida de Peso / Ensayos Clínicos Controlados Aleatorios como Asunto / Programas de Reducción de Peso Límite: Adult / Female / Humans Idioma: En Revista: Trials Asunto de la revista: MEDICINA / TERAPEUTICA Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido