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Study into the feasibility and effectiveness of a personalised lifestyle intervention (LIFE-ID intervention) in achieving long-term lifestyle improvement in adults with intellectual disabilities

Study into the feasibility and effectiveness of a personalised lifestyle intervention (LIFE-ID intervention) in achieving long-term lifestyle improvement in adults with intellectual disabilities - LEEV! Intervention study for adults with intellectual disabilities

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON56799
Enrollment
80
Registered
2023-10-12
Start date
2024-07-05
Completion date
Unknown
Last updated
2026-03-16

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

Conditions

Some synonyms include: - Behavioral health risks

Interventions

Participants will follow a 6 month personalised lifestyle intervention targeting physical activity and diet quality. The intervention involves changes at an intrapersonal, interpersonal and location l

Sponsors

Hanze University of Applied Sciences Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: • Having an intellectual disability according to the international definition; • Eighteen years of age or older; • Having a lifestyle-related query; • Residing at or receiving support from one of the participating healthcare organisations; • Written informed consent from the participants themselves or a legal representative.

Exclusion criteria

Exclusion criteria: Participants will be excluded if they exhibit any of the following exclusion criteria shortly prior to entering the study:  - Severe mental or physical health issues that prevent the participant from taking part. The physicians, and behavioural scientists of the potential participant will evaluate whether the health condition of the potential  participant requires exclusion from the study. In the end, the decision about in- or exclusion will be made in consultation between the physicians, behavioural scientist, representatives and principal researchers.

Design outcomes

Primary

MeasureTime frame
The main study outcome is change in physical activity.

Secondary

MeasureTime frame
Study outcomes on an intrapersonal level Anthropometry/body composition • Height (cm from standing position, or using knee height) • Body weight (kg)  • Body Mass Index (kg/m2) • Waist circumference (cm, standing up or in supine position) • Hip circumference (cm) • Waist to hip (ratio) • Muscle mass (%, kg), fat mass (%, kg), fat free mass and total body water Physical fitness: • 30 seconds Chair stand and 5 times Chair stand • Grip strength (kg) • Static balance test • Comfortable walking speed Questionnaires: • Dietary quality • ID-Frailty Index Short Form • Anxiety, Depression And Mood Scale • The Aberrant Behaviour Checklist Study outcomes an interpersonal level Questionnaires: • ADSP-HENU • ADSP-HEPA • The Usefulness, Satisfaction, and Ease of Use Questionnaire • The System Usability Scale Study outcomes on an organisational level Questionnaire: • DIHASID • MIDI-ID

Countries

Netherlands

Contacts

Public ContactA. Waninge

Hanze University of Applied Sciences Groningen

a.waninge@pl.hanze.nl050-5953539

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Mar 20, 2026