Actively Recruiting
LIVES: Personalized Lifestyle Intervention for Patients With Depression
Led by University Medical Center Groningen · Updated on 2024-05-08
38
Participants Needed
2
Research Sites
273 weeks
Total Duration
On this page
Sponsors
U
University Medical Center Groningen
Lead Sponsor
G
GGZ Drenthe Mental Health Institution
Collaborating Sponsor
AI-Summary
What this Trial Is About
Persons with affective disorder have a considerably increased risk of cardiovascular disease. To a considerable extent, this is due to an unhealthy life style. At present, no adequate lifestyle interventions are available for these patients. In the present pilot intervention study we study the acceptability and feasibility of a newly developed lifestyle intervention that is specifically tailored to the needs of patients with affective disorders treated in mental health care or general practice.
CONDITIONS
Official Title
LIVES: Personalized Lifestyle Intervention for Patients With Depression
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Outpatients diagnosed with chronic bipolar disorder (type I or II) or chronic/recurrent severe depression
- Receiving psychopharmacological treatment
- Physical and lifestyle monitoring showing three or more metabolic parameters outside normal range (mental health care patients only)
- Diagnosis of depressive symptoms or disorder in the past year registered in general practice (GP patients only)
- At least mild depressive symptoms (Beck Depression Inventory-II score ≥14) (GP patients only)
- Body mass index ≥25 kg/m2 or increased waist circumference (>88cm for women, >102cm for men) (GP patients only)
- 18 years or older and able to participate as confirmed by treating physician
- Availability of one or two close support persons (friends or family) to act as a buddy
You will not qualify if you...
- Current treatment in mental health care (GP patients only)
- Severe somatic or neurological disease at GP's discretion (GP patients only)
- Currently participating in another lifestyle intervention
- Insufficient proficiency in Dutch
- Unable to read and write
AI-Screening
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Trial Site Locations
Total: 2 locations
1
GGZ Drenthe
Assen, Drenthe, Netherlands, 9404 LA
Actively Recruiting
2
University Medical Center Groningen
Groningen, Netherlands, 9700 AD
Actively Recruiting
Research Team
H
Huibert Burger, MD PhD
CONTACT
E
Edith Liemburg, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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