CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 184 enrolled
Drug / intervention
Intervention Groupother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06988566
NCT06988566N/ACompleted

Telemedical Monitoring and Treatment of COPD Patients Associated With General Practice (TEMOKAP)

ECM Klinikken APS·interventional·Posted May 25, 2025·Updated Jun 3, 2025

In Brief

A clinical study evaluating Intervention Group for COPD (Chronic Obstructive Pulmonary Disease). Completed, enrolled 184 participants across 1 site.

Detailed Summary

The purpose of this study (The TEMOKAP study) is to investigate whether home-based treatment with telemedicine and support from healthcare professionals can prevent acute exacerbations of COPD and avoid acute hospital admissions, and whether this will improve the participant's health status and quality of life. In other words, the project seeks to document how life with COPD can be made better and safer for all COPD patients. The project is a collaboration between the University of Copenhagen, alles Lægehus (everyone's medical practice), Epital Health A/S, and Apopro.dk and will be conducted as a scientific study.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesDenmark
Collaborators--

Timeline

N/ACompletedFinished
202120222023202420252026
First PostedMay 25, 2025
Enrollment StartSep 4, 2020
Primary CompletionJul 1, 2022
Study CompletionSep 2, 2022
TodayJul 2, 2026
Enrollment to primary: 1.8 yearsPosted 1.1 years ago

Interventions

Intervention Groupother

The intervention were connected to the ECM response and coordination centre (RCC) which provided the participants with 24/7/365 access to assistance from certified RCC staff who were supported by eDoctors. Patients self-tracking activities (saturation, pulse, lung function, temperature and report on increased sputum, coughing, and shortness of breath) were monitored dayly by the RCC whoom would contact them in the event of signs of deterioration. The RCC staff together with the participant would make informed decisions, via phone or video call, on how to best manage the change in condition guided by the previous measures evaluated with graphs, including plotted trends. If there was a need for medical treatment, a treatment plan was drawn up with fixed follow-ups and a course plan.