Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT06628011

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

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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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

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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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