I-WEAR: Evaluating Wearables and Health Summaries in ICU Survivors

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorLudwig Boltzmann Gesellschaft

About this trial

This pilot study investigates the use of wearable health technology and bi-weekly digital health summaries in patients recovering from intensive care. Many patients experience physical, psychological, and cognitive challenges after an ICU stay, a condition known as Post-Intensive Care Syndrome (PICS). The study aims to evaluate the feasibility and usability of wearable devices-such as smartwatches, blood pressure monitors, and smart scales-for tracking recovery in real-world settings.

Participants will be randomly assigned to one of three groups: standard ICU follow-up care, wearable use only, or wearable use combined with bi-weekly health reports and optional lifestyle consultations. The study will assess participants' quality of life, experience using the technology, and adherence over a 6-month period. Results will inform the future use of digital tools in post-ICU care.

Eligibility criteria

Qualifiers

Age 18-65 years at the time of ICU admission

ICU stay of at least 48 hours

ICU discharge within the last 2 years

Comorbidity of diabetes mellitus and/or chronic heart failure/coronary artery disease

Disqualifiers

Presence of a legal guardian

No smartphone or internet access

No cardiovascular disease/event and/or diabetes

Implanted pacemaker or defibrillator

Trial design

Treatments tested in this trial

  • Wearable Health Monitoring
  • Digital Health Summary and Lifestyle Counseling

Treatment groups

60 Participants
are divided into 3 treatment groups

Sponsors and collaborators