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The feasibility, acceptability and preliminary effectiveness of a combined lifestyle intervention for outpatients with a severe or chronic psychiatric illness (CHAPTER): a pilot controlled trial

The feasibility, acceptability and preliminary effectiveness of a combined lifestyle intervention for outpatients with a severe or chronic psychiatric illness (CHAPTER): a pilot controlled trial - CHAPTER pilot study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON52338
Enrollment
24
Registered
2021-10-04
Start date
2022-01-03
Completion date
Unknown
Last updated
2024-06-18

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

Conditions

Mental disorder psychiatric disorder

Interventions

Sponsors

Lentis (Groningen)
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: All participants are: -Patients treated in the outpatient clinics of Lentis -Treated in specialistic mental health care for at least six months -Adult (18+) -In relative stable phase -Capable to read, write and speak in the Dutch language -Available and capable to attend the intervention at set moments and locations -Capable to follow the research procedures

Exclusion criteria

Exclusion criteria: -Main diagnosis of autism spectrum disorder, psychotic disorder, eating disorder or obsessive compulsive disorder -Current crisis, severe symptoms, suicidality, self-mutilation or distorted reality -Insufficient online skills to attend an online training through video calling, despite facilitation by the research team -Participation in a combined lifestyle intervention or lifestyle treatment in the past year -Other implications for lifestyle interventions that cannot be overcome (e.g. due to physical illness, use of certain medication such as clozapine or intellectual disability) -No informed consent provided

Design outcomes

Primary

MeasureTime frame
The main goal of the pilot trial is to evaluate the feasibility and acceptability of the intervention and to evaluate and improve the intervention and research protocol.

Secondary

MeasureTime frame
To explore the preliminary efficacy of the intervention, we will examine the effect of the intervention on several health indicators and lifestyle behavior.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)