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Clinical Trials/NCT04373070
NCT04373070
Completed
Not Applicable

CAir: Quality-of-Life Management for COPD Patients

University of Zurich1 site in 1 country35 target enrollmentFebruary 3, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Copd
Sponsor
University of Zurich
Enrollment
35
Locations
1
Primary Endpoint
Health-related quality-of-life (HrQoL)
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The investigators aim to investigate the effects of a telemonitoring and chatbot-based application of "Living well with COPD" (CAir) on health-related quality-of-life in patients with COPD.

Detailed Description

The disease management programme "Living well with COPD" was developed to relieve symptoms and prevent exacerbations. It covers a disease self-management approach, educational topics, lifestyle coaching and physical activity advice. Future implications should aim to make the intervention easily accessible for a broad spectrum of patients at scalable costs. Patients need an engaging communication platform which can inform, coach and even listen in between medical visits. The inclusion of a chatbot agent may provide this tailored feedback. The investogator's aim is to investigate the effects of a telemonitoring and chatbot-based application of "Living well with COPD" on health-related quality-of-life in patients with COPD.

Registry
clinicaltrials.gov
Start Date
February 3, 2021
End Date
May 30, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Diagnosed COPD according to GOLD-guidelines

Exclusion Criteria

  • Physical or intellectual impairment precluding informed consent or protocol adherence
  • Non-German speaking
  • Acute or recent (within the last 6 weeks) exacerbation of COPD
  • Attending a pulmonary rehabilitation program within the last 3 months
  • Pregnant patients

Outcomes

Primary Outcomes

Health-related quality-of-life (HrQoL)

Time Frame: 3 months

St. George Respiratory Questionnaire (SGRQ). Scoring: Scores range from 0 to 100, with higher scores indicating more limitations.

Secondary Outcomes

  • Symptom burden(3 months)
  • Spirometry(3 months)
  • Accelerometry(3 months)
  • Functional exercise capacity(3 months)

Study Sites (1)

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