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Improving physical health and lifestyle behaviors in patients with serious mental illness: a cluster randomized controlled trial on the effectiveness of the nurse-led GILL eHealth intervention

Improving physical health and lifestyle behaviors in patients with serious mental illness: a cluster randomized controlled trial on the effectiveness of the nurse-led GILL eHealth intervention - GILL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON53725
Enrollment
258
Registered
2022-07-06
Start date
2024-05-23
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Serious mental illness, chronic psychiatric disorder

Interventions

The provided intervention is the nurse-led GILL eHealth. This eHealth contains two modules: OurGILL and MyGILL. OurGILL focuses on systematic somatic screening and provides an overview of all somatic

Sponsors

Amsterdam UMC
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Diagnosis of schizophrenia, other psychotic disorder and/or disorders defined as serious mental illness according to Delespaul consensusgroup at Maastricht University  - Aged from 18 and older - Body mass index (BMI) >= 27 - Access and ability to use internet

Exclusion criteria

Exclusion criteria: - Contra-indications (to be assessed by the threating physician/psychiatrist) for participation due to acute psychiatric crisis or severe somatic diseases - Pregnancy or breastfeeding in women at the time of inclusion - Subjects with a cognitive impairment sufficient to interfere with their ability to provide informed consent, complete study questionnaires, or participate in the intervention - Subject not able to communicate in the Dutch language

Design outcomes

Primary

MeasureTime frame
The primary study parameter is the metabolic syndrome severity, which is operationalized by the Metabolic Syndrome Severity Score (MSSS).

Secondary

MeasureTime frame
Secondary study parameters are physical fitness, physical activity, perceived lifestyle behaviours, quality of life, recovery, psychosocial functioning, health related self-efficacy, health care utilization, and medication use.

Countries

Netherlands

Contacts

Public ContactM.M. Hoogervorst

Amsterdam UMC

m.m.hoogervorst@amsterdamumc.nl0629680823

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)