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Food related computerised attention training for obesity

A randomised controlled feasibility study of food related computerised attention training for obesity versus active (mindfulness-based intervention [MBI] and waiting list control [FOCUS])

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN15745838
Enrollment
45
Registered
2018-05-22
Start date
2018-10-01
Completion date
Unknown
Last updated
2023-04-24

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

Conditions

Overweight/obesity Nutritional, Metabolic, Endocrine Obesity

Interventions

After baseline assessment, participants will be randomly allocated to either Attention Bias Modification Training (ABMT), Mindfulness, Based Intervention (MBI) or a waiting list condition. To balance

Sponsors

King's College London
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Male or female participants 2. 18 years old or older (women of childbearing age will be included) 3. BMI of >25kg/m2 4. Fluent in English 5. Informed consent (written and witnessed)

Exclusion criteria

Exclusion criteria: 1. Having a current other major psychiatric disorder (e.g., major depression, major suicidality, substance dependence, psychosis) needing treatment in its own right 2. Having a diagnose of Anorexia Nervosa, Bulimia Nervosa or Eating disorder not otherwise specified (EDNOS) 3. Diagnosis of Diabetes Mellitus 4. Having recently started psychotropic medication or increased the dose (i.e. within the previous 2 weeks) 5. Taking medication for weight loss 6. Pregnancy (either current or during the past 6 months) 7. Regular current or past mindfulness meditation or yoga practice (defined as > 20 minutes, twice or more times per week during the past 2 months). 8. Visual impairments that cannot be corrected with contact lenses or glasses

Design outcomes

Primary

MeasureTime frame
1. The feasibility of conducting a large scale RCT of attention trainings in overweight/obese patients by assessing recruitment, attendance, and retention rates. An acceptability and credibility questionnaire will be administered at post-assessment (i.e., week 8) 2. The quality, completeness, and variability of the outcome measures, determined using descriptive statistical analyses and graphical methods

Secondary

MeasureTime frame
Weight, eating behaviour and cognition before and after trainings. Assessment of these outcome measures will include different self-report questionnaires: 1. Hunger, craving, mood, stress and anxiety levels, measured using the Visual Analogue Scale (VAS) 2. Eating behaviour and awareness, assessed using the Food Craving Questionnaire – Trait version (FCQ-T), the Eating Disorders Examination Questionnaire (EDEQ), the Power of Food scale, the Mindful Eating Questionnaire (MEQ) and Mindful Awareness and Attention Scale (MAAS) 3. General psychopathology measured using the Depression, Anxiety and Stress Scale (DASS-21) and the State and Trait Anxiety Inventory (STAI) 4. Quality of diet and calorie intake assessed using 24h dietary recall questionnaire 5. BMI and body composition calculated by taking height and weight on the day of the assessment using a bioelectrical impedance scale 6. Different components of attention (i.e. alerting, orienting and executive attention) assessed by the food-Attention Network Task (Food-ANT) 7. Attention bias for food, measured by a dot-probe task while recording eye movements 8. Preference of low vs high-calorie food items, assessed using the food-choice task 9. State levels of cue-elicited food cravings, assessed using the Food Challenge Task 10. Food intake measured by the Bogus Taste Test, where participants will be asked to rate different kinds of highly palatable food in terms of their visual attractiveness, smell and taste and will be told that they should try as much of the offered items as they like. Food consumption will be determined by weighing remaining food.? All of these measures will be taken both at baseline assessment and post-assessment (8 weeks) with the exception of the EDEQ and the Power of Food Scale, which will also be completed by participa

Countries

England, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 28, 2026