Actively Recruiting
The Evira Study: Additional Support During Obesity Treatment
Led by Karolinska Institutet · Updated on 2026-05-05
40
Participants Needed
2
Research Sites
63 weeks
Total Duration
On this page
Sponsors
K
Karolinska Institutet
Lead Sponsor
E
Evira AB
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this clinical trial is to evaluate the effect of adding a digi-physical treatment tool as a complement to the local treatment with obesity medication in adolescents with obesity. The main question it aims to answer is: \- Can a combination of a digi-physical treatment tool and obesity medication improve treatment outcomes for patients with obesity compared to patients treated with obesity medications alone? This is a randomized controlled two-arm multicenter study where participants will be randomized to the intervention group (digi-physical treatment+medication) or control group (medication only). Participants will be followed for six months.
CONDITIONS
Official Title
The Evira Study: Additional Support During Obesity Treatment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients offered liraglutide or semaglutide according to the clinic's routines
- Aged 12 to 17 years at the time of inclusion
- Family agrees to participate in the clinical study
You will not qualify if you...
- Endocrine disorders other than well-controlled hypothyroidism
- Severe neuropsychiatric disorders that may affect adherence to the study
- Eating disorder requiring treatment within the last six months before inclusion or observed during screening
- Somatic conditions that may complicate evaluation, such as irregular oral corticosteroid treatment
- Hypothalamic or monogenic obesity, and genetic syndromes such as Down syndrome
- Patients deemed unsuitable for participation by the responsible physician
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 2 locations
1
HKH Crown Princess Victoria's Childrens and youth Hospital Linköping
Linköping, Sweden
Actively Recruiting
2
Ystad lasarett, Barn och ungdomsmedicinmottagningen
Ystad, Sweden
Actively Recruiting
Research Team
P
Pernilla Danielsson Liljeqvist, Associate Professor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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