Actively Recruiting
Digital Follow-up of Aerobic Interval Training in Outpatients With Mental Disorders
Led by Norwegian University of Science and Technology · Updated on 2025-04-01
40
Participants Needed
1
Research Sites
295 weeks
Total Duration
On this page
Sponsors
N
Norwegian University of Science and Technology
Lead Sponsor
S
St. Olavs Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
This randomized-controlled trial (RCT) will investigate if digital follow-up of exercise, i.e. followup through the new citizen portal HelsaMi, coupled with an exercise app can result in exercise adherence and improved oxygen uptake in individuals with mental disorders (MD). Secondary, the project will provide information regarding effects on cardiovascular disease risk-factors, functional capacity, quality of life, satisfaction, and cost through a randomized-controlled trial (RCT) including individuals with MDs. Outcomes assessed in this project, such as maximal oxygen uptake, functional capacity, and quality of life, are strongly related to the ability to carry out activities of daily living. These outcomes are associated with benefits such as reduced sick leave, extended life expectancy, independence, and improved health status with increasing age. Economically, with the world population growing older and health care resources being stretched, there is clearly a need to apply and evaluate effective alternative methods to improve somatic health on a broader scale in a sustainable fashion, preferably utilizing existing platforms and exercise apps.
CONDITIONS
Official Title
Digital Follow-up of Aerobic Interval Training in Outpatients With Mental Disorders
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Individuals receiving outpatient mental health treatment at St. Olavs Hospital
- Aged 18 to 65 years
- Both men and women able to carry out exercise training
- Capable of giving informed consent and using the HelsaMi digital platform
You will not qualify if you...
- Contraindications for exercise training and testing per ACSM guidelines
- Life-threatening or terminal medical conditions
- Unable to carry out intervention or test procedures
- Pregnant or mothers less than 6 months postpartum
- Inpatients at an acute psychiatric ward
- Planned surgery interfering with the intervention
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
St. Olavs Hospital HF. And NTNU (Norwegian University of Science and Technology) Department of Mental Health, Faculty of Medicine and Health Sciences
Trondheim, Norway
Actively Recruiting
Research Team
T
Torgeir F Fredriksen Ektvedt, PhD Candidate
CONTACT
M
Mona Nygård, Postdoc
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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