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HEalth Promotion Intervention in MEntal Health Care

Effectiveness and Cost-effectiveness of a Health Promotion Intervention Targeting Physical Activity and Eating Habits in Persons With Mental Disorders

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01336946
Acronym
HEPIMEC
Enrollment
742
Registered
2011-04-18
Start date
2011-01-31
Completion date
2013-05-31
Last updated
2014-12-05

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

Conditions

Unhealthy Lifestyle of Persons With Mental Disorders

Keywords

lifestyle, mental disorder

Brief summary

Overweight and obesity have become a serious global public health problem and the prevalence of these conditions is even higher among persons with mental disorders, compared with the general population. Overweight and obesity are partially associated with sedentary lifestyles and unhealthy eating habits. The aim of the study is to examine the effectiveness and cost-effectiveness of a health promotion intervention targeting physical activity and eating habits in persons with mental disorders. The study hypothesis is that between baseline and the end of the intervention, and after a 6-month follow up period, significant differences in the primary and secondary outcomes between the intervention and control group will be identified. The investigators also hypothesize that the health promotion intervention will be cost-effective.

Interventions

BEHAVIORALPsycho educational and behavioural group sessions

10 psycho educational and behavioural group sessions on topics like the Food Triangle, healthy eating, the importance of physical activity, healthy eating on a limited budget, implementing physical activity into the daily life, the influence of advertisements...

BEHAVIORALWalking session

A weekly supervised walking session (30 minutes) in a 10-week period.

Sponsors

University Ghent
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 18 years of age or older * living in sheltered housing * diagnosed according to the Diagnostic and Statistical Manual of mental disorders (DSM-IV manual)

Design outcomes

Primary

MeasureTime frameDescription
change in body weight 10 weeks post-interventionafter 10 weeksThe primary outcome of the study consists of changes in body weight between baseline and 10-weeks post-intervention in the intervention and control group separately and between the intervention and the control group.The participants will be weighed in light clothing without shoes, with standardised measurement.
change in body weight 26 weeks post-interventionafter 26 weeksThe primary outcome of the study consists of changes in body weight between baseline and 26-weeks post-intervention in the intervention and control group separately and between the intervention and the control group.The participants will be weighed in light clothing without shoes, with standardised measurement.

Secondary

MeasureTime frameDescription
Waist circumference, 10 weeks post-interventionAfter 10 weeksWaist circumference, assessed by using a tape measure.
Waist circumference, 26 weeks post-interventionAfter 26 weeksWaist circumference, assessed by using a tape measure.
Quality of Life, 10 weeks post-interventionAfter 10 weeksQuality of life, assessed by using the SF-36 Health Survey.
Quality of Life, 26 weeks post-interventionAfter 26 weeksQuality of life, assessed by using the SF-36 Health Survey.
Levels of physical activity, 10 weeks post-interventionAfter 10 weeksLevels of physical activity, assessed by using the International Physical Activity Questionnaire long version (IPAQ) and by using pedometers.
Body Mass Index 10 weeks post-interventionafter 10 weeksBody Mass Index, calculated as the weight in kilograms divided by the square of the height in metres (kg/m²)
Eating habits, 10 weeks post-interventionAfter 10 weeksEating habits, assessed by using a 24-hour dietary recall.
Eating habits, 26 weeks post-interventionAfter 26 weeksEating habits, assessed by using a 24-hour dietary recall.
Psychiatric symptom severity, 10 weeks post-interventionAfter 10 weeksPsychiatric symptom severity, assessed by using the Brief Symptom Inventory (BSI).
Psychiatric symptom severity, 26 weeks post-interventionAfter 26 weeksPsychiatric symptom severity, assessed by using the Brief Symptom Inventory (BSI).
Levels of physical activity, 26 weeks post-interventionAfter 26 weeksLevels of physical activity, assessed by using the International Physical Activity Questionnaire long version (IPAQ) and by using pedometers.
Body Mass Index, 26 weeks post-interventionafter 26 weeksBody Mass Index, calculated as the weight in kilograms divided by the square of the height in metres (kg/m²).

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026