Obesity Nutritional, Metabolic, Endocrine Obesity
Conditions
Interventions
Participants are randomized to one of two groups using web-based randomisation software (https://www.randomizer.org/).
Motivational Interviewing (MI) group:
Participan
Sponsors
NIHR CLAHRC Southwest Peninsula (PenCLAHRC)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. BMI of or above 25 2. Females and males 3. Must be age 18 or above
Exclusion criteria
Exclusion criteria: 1. Pregnancy 2. History of eating-disorders
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Weight loss is determined by measuring weight (kg) and waist circumference (cm) at baseline, 6 and 12 months. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Physical activity is measured using the International Physical Activity Questionnaire (IPAQ-short) during session one and one week before follow up at six months 2. Diet is measured using the Food Frequency Questionnaire during session one and one week before follow-up at six months 3. Use of goal imagery is measured using the Thought Frequency Scale at home baseline, one week before session one and the first booster call at the end of trial week four 4. Quality of Life is measured using the QoLIAD (Global Quality of Life Assessment) during session one and one week before follow-up at six months 5. Treatment expectancy/credibility is measured using Credibility/Expectancy Questionnaire after the second session at the end of week two 6. Self-efficacy for exercise is measured using Exercice Self-Efficacy Scale (SCI) one week before session one (lab baseline) at home baseline and at the end of week four after the first booster call 7. Participant experience is measured using the participant experience questionnaire at follow-up 8. Self-efficacy for diet is measured using WELQ (Weight Efficacy Lifestyle Questionnaire) | — |
Countries
United Kingdom
Contacts
Public ContactLinda Solbrig
Outcome results
None listed