Digital Follow-up of Aerobic Interval Training in Outpatients With Mental Disorders

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorNorwegian University of Science and Technology

About this trial

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.

Eligibility criteria

Qualifiers

Individuals receiving outpatient mental health treatment at the clinics of mental health at St. Olavs Hospital,.

Both men and women able to carry out exercise training.

Participants must be capable of giving informed consent and use HelsaMi.

Disqualifiers

Contraindications for exercise training and testing according to the ACSM specifications; life-threatening or terminal medical conditions; unable to carry out intervention or test procedures; pregnancy; mothers <6 months post-partum.

Inpatients at an acute psychiatric ward or have any planned surgery that would interfere with the intervention.

Trial design

Treatments tested in this trial

  • Intervention group/training group

Treatment groups

40 Participants
are divided into 2 treatment groups

Locations

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

Sponsors and collaborators

Norwegian University of Science and Technology

Lead sponsor

St. Olavs Hospital

Collaborator

Molde University College

Collaborator