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Feasibility Study of a Digital Interactive Life-style Platform for Individuals After Rehabilitation

NCT07597031 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 240

Last updated 2026-05-19

No results posted yet for this study

Summary

The goal of this clinical trial is to evaluate the feasibility and usability of a digital lifestyle platform designed to support patients after discharge from inpatient rehabilitation. It will also assess patient engagement and the potential of the platform to support long-term self-management and healthy lifestyle behaviors in an outpatient setting.

The main questions it aims to answer are:

Is the platform feasible and acceptable for patients after rehabilitation? Do patients engage with and regularly use the platform over time? Can personalized digital recommendations support adherence to healthy behaviors and self-management?

Researchers will evaluate a telemedicine platform that delivers individualized suggestions, including lifestyle applications, educational content, and advice from healthcare professionals. The content is tailored to patient needs and continuously adapted based on patient feedback.

Participants will:

Use the digital platform after discharge from inpatient rehabilitation for a defined follow-up period Receive personalized recommendations through the platform Rate the usefulness of recommendations to enable continuous adaptation Attend study visits or remote assessments to evaluate usability, engagement, and outcomes Continue standard outpatient care alongside the intervention

Conditions

  • Chronic Obstructive Pulmonary Disease (COPD)
  • Acute Coronary Syndrome
  • Fragility Fracture
  • Minor Stroke

Interventions

BEHAVIORAL

Digital Lifestyle Platform

Patients are going to use the Digital Lifestyle Platform for six months.

BEHAVIORAL

Usual Care (Standard Post-Rehabilitation Care)

Patients are going to follow their post-rehabilitation care plan without access to the platform

Sponsors & Collaborators

  • Matthias Wilhelm, MD

    lead OTHER

Principal Investigators

  • Matthias Wilhelm, Prof. Dr. med. · Center for Rehabilitation & Sports Medicine, Berner Reha Zentrum and Inselspital, Bern University Hospital, University of Bern

  • Thimo Marcin, PhD · Center for Rehabilitation & Sports Medicine, Berner Reha Zentrum and Inselspital, Bern University Hospital, University of Bern

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-05-01
Primary Completion
2027-02-01
Completion
2027-02-01

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07597031 on ClinicalTrials.gov