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Remotely Monitored and Coached Cardiac Rehabilitation Northern Sweden

Remotely Monitored and Coached Exercise Based Cardiac Rehabilitation in Northern Sweden l

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03479957
Acronym
RECREATION
Enrollment
90
Registered
2018-03-27
Start date
2019-02-03
Completion date
2024-02-28
Last updated
2023-05-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Defects, Congenital

Brief summary

Supervised exercise is an essential component of contemporary center-based cardiac rehabilitation (CR) programs. Despite the proven effectiveness, uptake and adherence to supervised exercise-based CR (exCR) remains suboptimal (approximately 50%), especially in rural and remote areas of Sweden. The main reasons for low participation rate in centre-based exCR are different accessibility barriers i.e. long distances, transportation problems or employment commitments. In this randomised clinical trial, the overall aim is to evaluate the effectiveness of, home-based, remotely monitored and coached exCR using the REMOTE-CR system compared to home-based exCR based on individualized information regarding current exercise recommendations but without monitoring and coaching (usual care) to improve exercise capacity. Our hypothesis is that remotely monitored and coached exCR will improve exercise capacity to a greater extent than home-based exCR without monitoring and coaching (usual care).

Interventions

BEHAVIORALREMOTE-CR

The patients randomized to remotely monitored exercise can either work out with self-selected activities e.g. Nordic-walking, cycling, skiing or participate in supervised exercise session via video link. Remotely monitored exercise training sessions will be offered monday-friday 13.00-16.00.

OTHERControl

The patients randomized to be controls will receive individualized information and instructions regarding current exercise recommendations but will not be monitored or coached during their exercise sessions (usual care)

Sponsors

Umeå University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Scheduled appointment with physiotherapist for follow-up after cardiac event: ----Myocardial Infarction (MI) * Per cutaneous coronary intervention (PCI) due to MI or angina pectoris * Open heart surgery due to coronary artery disease or valvar disease * Living in the catchment area of Heart centre, University Hospital of Umeå.

Exclusion criteria

* Clinically unstable * Postoperative infection * Comorbidity affecting ability to participate in exCR

Design outcomes

Primary

MeasureTime frameDescription
Change in submaximal aerobic exercise capacityBaseline and 12 weeksThe aerobic exercise capacity (W) will be evaluated using a standardised submaximal exercise test on cycle ergometer

Secondary

MeasureTime frameDescription
Self-reported physical activity using the physical activity scale br Frändin and GrimbyBaseline and 12 weeksThe Activity scale by Frändin and Grimby describes 6 levels of physical activity. The scale includes 6 items that ranges from 1 indicating mostly physically inactive to 6 indicating a very high physical activity level.
Kinesiophobia (fear of movement)Baseline and 12 weeksThe Swedish version of the Tampa scale for Kinesiophobia Heart (TSK-SV Heart) The scale comprises 17 items assessing subjective rating of kinesiophobia. The total score varies between 17-68 and a score \>37 defines a high level of kinesofobia.
Muscle endurance capacityBaseline and 12 weeksNumber of repetitions achieved during test of Unilateral isotonic shoulder flexion and Unilateral isotonic heel-lift
Isometric grip strengthBaseline and 12 weeksIsometric grip strength will be evaluated using a hydraulic hand dynamometer
Self-reported physical activity using theInternational Physical Activity QuestionnaireBaseline and 12 weeksInternational Physical Activity Questionnaire: Results will be presented as a continuous variable, total metabolic equivalent (MET) minutes per week, where a higher score indicates a higher physical activity level. Result will also be presented as a categorical variable: High Physical activity level: achieving a total physical activity of at least 3000 MET-minutes/week. Moderate physical activity: achieving a minimum of at least 600 MET-minutes per week. Low physical activity level: not achieving the minimum of 600 MET minutes per week

Other

MeasureTime frameDescription
Evaluation of change the participation rate in supervised cardiac rehabilitation12 weeksEvaluation of change the participation rate can be enhanced using the REMOTE -CR system
Patients experiences of REMOTE-CR and and exercise led via video link12 weeksThe study participants experience of the REMOTE-CR system and exercise sessions via video link will be evaluated using a questionnaire

Countries

Sweden

Contacts

Primary ContactCamilla Sandberg, PhD
camilla.sandberg@umu.se+46907858441
Backup ContactHelena Cronesten, RPT
+46907858441

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026