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Clinical Trials in Switzerland / NCT06516172
Recruiting Observational

The Bern Rehab Registry

NCT06516172 · tracked via the Priya Life Science Switzerland tracker
Phase
Observational
Started
2020-12-01
Last updated
2024-08-19

Condition(s) studied

CancerCardiovascular DiseasesMusculoskeletal DiseasesPulmonary Disease

Investigational drug(s) / intervention(s)

Comprehensive disease-specific rehabilitation

Comprehensive disease-specific rehabilitation: Participation in (a) inpatient rehabilitation, (b) outpatient centre-based, (c) outpatient digitally-enhanced centre- and home-based, or (d) outpatient home-based digital/tele rehabilitation. Duration is 3 weeks for inpatient and 12 weeks for outpatient programmes.

Study summary

This study examines the health outcomes of patients with long-term illnesses such as cancer, heart, lung, or musculoskeletal diseases who participate in a rehabilitation programme. The programme may involve staying in a facility (inpatient), visiting a facility (outpatient), home-based care supported by digital health tools (telerehabilitation), or a combination of facility- and home-based options.

The key health outcomes being measured include physical fitness and strength, body composition (like body fat and muscle mass), specific risk factors related to the diseases, and patients' self-reported health and experience outcomes, such as feelings of anxiety, depression, fatigue, overall quality of life, and satisfaction with the rehabilitation programme.

These measurements provide important information about the patients' lung, heart, and muscle health, as well as their mental well-being. They also help to predict the likelihood of further health complications, the chance of needing to be hospitalized again, and overall quality of life. This information is useful for improving the quality of care, tailoring future provision of rehabilitation services and long-term care for patients with chronic conditions.

Additionally, the study will provide insights into how new technologies like telerehabilitation are implemented, including how well they are adopted, followed, and accepted by patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients aged 18 years and older with a chronic non-communicable disease * Signed general informed consent * Referral to a comprehensive disease-specific rehabilitation program Exclusion Criteria: * Refuted or missing general informed consent for further use of health-related data and samples.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Berner Reha Centre, Centre for Rehabilitation & Sports Medicine, Insel Group Heiligenschwendi Canton of Bern Recruiting
Reha Inselspital, Bern University Hospital, Centre for Rehabilitation & Sports Medicine, Insel Group Bern Switzerland Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06516172 on ClinicalTrials.gov ↗ ← All trials in Switzerland