Use of E-health Based Exercise Intervention After COVID-19 | NCT05770505

Studies
Use of E-health Based Exercise Intervention After COVID-19

NCT05770505

Sponsor

Norwegian University of Science and Technology

Status

Completed

Last Update Posted

Jan 5, 2026Actual

Enrollment

77Actual

Phase

Not Applicable

Conditions

COVID-19

Interventions

Exercise training using an e-health tool

Countries

Norway

Protocol Section

Identification Module Status Module Sponsor/Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms/Interventions Module Outcomes Module Eligibility Module Contacts/Locations Module References Module IPD Sharing Statement Module

Results Section

Participant Flow Module Baseline Characteristics Module Outcome Measures Module Adverse Events Module More Info Module

Annotation Section

Annotation Module

Document Section

Large Document Module

Derived Section

Miscellaneous Info Module Condition Browse Module Intervention Browse Module

Protocol Section

Identification Module

NCT ID

Results Section

No data available

No data is available for this block.

Annotation Section

No data available

No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Version Holder

Status Module

Record Verification Date

Dec 2025

Overall Recruitment Status or Expanded Access Status

Completed

Last Known Status

Not provided

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

Apr 17, 2023Actual

Primary Completion Date

May 31, 2024Actual

Completion Date

Dec 31, 2024Actual

First Submitted Date

Mar 13, 2023

First Submission Date that Met QC Criteria

Mar 13, 2023

First Posted Date

Mar 15, 2023Actual

Results Waived

Not provided

Results First Submitted Date

Not provided

Results First Submitted that Met QC Criteria

Not provided

Results First Posted Date

Not provided

Certification/Extension (aka Delayed Results) First Submitted Date

Not provided

Certification/Extension First Submitted that Passed QC Review

Not provided

Certification/Extension First Posted Date

Not provided

Last Update Submitted Date

Dec 30, 2025

Last Update Posted Date

Jan 5, 2026Actual

Name	Class
University of Oslo	OTHER

Oversight Module

Has Data Monitoring Committee (DMC)

Is FDA Regulated Drug

Is FDA Regulated Device

Is Unapproved Device

Not provided

Pediatric Postmarket Surveillance of a Device Product

Not provided

Product Exported from US

Not provided

FDAAA801 Violation

Not provided

Description Module

Brief Summary

Reduced subjective and objective functional capacity performance are reported after COVID-19 in a large proportion of subjects. The aim of this study is to examine the feasibility and effect of using an e-health tool for guidance and tracking of exercise training in a general population of adults previously infected by COVID-19.

Detailed Description

Both hospitalized and non-hospitalized persons who have undergone extensive multi-disciplinary rehabilitation programs report significantly improved physical function after rehabilitation. Exercise training may be the key intervention to improve fitness and subjective complaints such as fatigue, low physical fitness and dyspnea after COVID-19 infection. However, traditional group-based exercise training or self-training programs at fitness centers have been shut down during the pandemic, and home-based interventions are warranted. To overcome the limitations and costs of a fitness center/personal trainer-based intervention study, more knowledge on the effectiveness and efficacy of using an e-Health system to recruit, train and monitor participants after illness are needed.

Design Module

Study Type

Interventional

Number of References to an Expanded Access Study

Not provided

Expanded Access Types

Not provided

Patient Registry

Not provided

Target Follow-Up Duration

Not provided

Phases

Not Applicable

Interventional Study Design

Allocation

Biospecimen

No data available

No data is available for this block.

Enrollment

77Actual

Arms/Interventions Module

Arm Groups

Label	Type	Description	Intervention Names
Supervised exercise	Experimental		Behavioral: Exercise training using an e-health tool
Control group	No Intervention

Interventions

Name	Type	Description	Arm Group Labels	Other Names
Exercise training using an e-health tool	Behavioral	Experimental: Exercise training will be guided by using the e-health tool MIA Health, with the possibility for digital communication between the participants and study personnel The participants will receive wearables that record heart rate. Participants will be encouraged to achieve 100 Activity Quotient (AQ) equivalents per week Control: No follow-up

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Cardiorespiratory fitness	Peak oxygen uptake	After 6 months intervention
Feasibilty	Measured as acceptability and adherence	After 6 months intervention

Secondary Outcomes

Measure	Description	Time Frame
Lung function	Spirometry	After 6 months intervention
Quality of life	Questionnaires (RAND-12)	After 6 months intervention

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

Inclusion Criteria:

Persons who have undergone COVID-19 disease
People who struggle to be physically active enough as a result of corona disease
People who experience reduced physical fitness as a result of corona disease

Exclusion Criteria:

-- more than 100 AQ per week (calculated from self-reported activity level)

uncontrolled hypertension (high blood pressure) (over 200/110).
symptomatic valve failure, hypertrophic cardiomyopathy, unstable angina, pulmonary
hypertension, heart failure and/or severe rhythm disturbances
cancer that makes participation impossible or exercise contraindicated. Considered individually in consultation with the attending physician.
chronic contagious infectious diseases.
Participates in other studies that are not compatible with participation in this project
Post-exertional symptom exacerbation (PESE)/post-exertional malaise (PEM)/post-exertional neuroimmune exhaustion (PENE).

Accepts Healthy Volunteers

Yes

Sex

All

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

18 Years

Maximum Age

59 Years

Standard Ages

Adult

Study Population

Not provided

Sampling Method

Not provided

Contacts/Locations Module

Central Contacts

Not provided

Overall Officials

Name	Affiliation	Role
Dorthe Stensvold Stensvold	Dorthe Stensvold, Professor, NTNU	Principal Investigator

Locations

Facility	Status	City	State	ZIP	Country	Contacts
Norwegian University of Science and Technology, Faculty of medicine, Department of circulation and medical imaging,		Trondheim		7006	Norway

IPD Sharing Statement Module

Plan to Share IPD

Undecided

Description

Not provided

Types

Not provided

Time Frame

Not provided

Access Criteria

Not provided

URL

Not provided

Condition Browse Module

MeSH Terms

ID	Term
D000086382	COVID-19

Ancestor Terms

ID	Term
D011024	Pneumonia, Viral
D011014	Pneumonia
D012141	Respiratory Tract Infections
D007239	Infections

Browse Leaves

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Browse Branches

Not provided