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
- Conditions
- Mental disorderpsychiatric disorder1003717610024450
- Registration Number
- NL-OMON52338
- Lead Sponsor
- entis (Groningen)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 24
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
-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
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The main goal of the pilot trial is to evaluate the feasibility and<br /><br>acceptability of the intervention and to evaluate and improve the intervention<br /><br>and research protocol.</p><br>
- Secondary Outcome Measures
Name Time Method <p>To explore the preliminary efficacy of the intervention, we will examine the<br /><br>effect of the intervention on several health indicators and lifestyle behavior.</p><br>