RecruitingNot ApplicableNCT06628011

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

Digital Follow-up of Exercise Training in Outpatients With Mental Disorders


Sponsor

Norwegian University of Science and Technology

Enrollment

40 participants

Start Date

Jan 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

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

Min Age: 18 YearsMax Age: 65 Years

Inclusion Criteria4

  • Individuals receiving outpatient mental health treatment at the clinics of mental health at St. Olavs Hospital,.
  • -18-65 years old
  • Both men and women able to carry out exercise training.
  • Participants must be capable of giving informed consent and use HelsaMi.

Exclusion Criteria2

  • 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.

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Interventions

OTHERIntervention group/training group

We will assess the short-term effects through a 12-week intervention, and its long-term effects after 1-year. Both the intervention group (IG) and control group (CG) will receive two sessions of aerobic interval training at the Exercise Training Clinic, situated at the Department of Psychosis and Rehabilitation, Psychiatry Clinic, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway. One training session consists of 36 minutes of high intensity training (HIT).


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

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NCT06628011


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