A Digital Health Intervention to Promote Self-management in Patients With Chronic Obstructive Pulmonary Disease

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-90
SponsorWestern Norway University of Applied Sciences

About this trial

Dyspnea, cough, and chronic mucus hypersecretion are common symptoms in patients with Chronic Obstructive Pulmonary Disease (COPD), which increases risk of infections followed by exacerbations, often leading to hospitalization, disease progression and mortality. This patient group requires lifelong treatment in healthcare. A mobile application was developed to facilitate adherence to evidence-based guidelines for tailored breathing and airway clearance techniques to enhance self-management. The app is only in Norwegian and has a Norwegian name which is "Pust Deg Bedre" (PDB). The PDB app is fully developed and tested and can be downloaded for free. The app seems promising as a treatment tool, but has not yet been clinical evaluated. This project aims to 1) explore the feasibility of providing the app for patients with COPD, 2) explore the patients' with COPD experiences with the use of the PDB-app in treating dyspnea and mucus secretion, 3) explore the physiotherapists' experiences with the use of the PDB-app in treating dyspnea and mucus secretion, 4) explore the physiotherapists' experiences with implementing the PDB-app in treatment of patients with COPD, 5) explore the patients' experiences with the education in use of the PDB-app, and 6) At a 6-month follow up: explore the physiotherapists experiences with the usefulness and applicability of PBD-app, and to generally explore their experiences with participating in the project.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Clinical diagnosis of Chronic Obstructive Pulmonary Disease

Mucus-related issues ≥3 times per week

Speak and write Norwegian

Ability to independently operate a smartphone and/or iPad

Disqualifiers

Severe mental illness

Substance abuse that hinder participation in the study

Trial design

Design model

Single group

Treatments tested in this trial

  • Digital health intervention by using a mobile application

    Device

    A digital health intervention for promoting self-management in patients with COPD by using a mobile application.

  • Feasibilty study and qualitative interview studies

    Other intervention

    This study is a one group feasibility study including quantitative and qualitative study designs. The investigators will use focus groups and indiviual interviews, as well as Interpersonal Process Recall (IPR) interviews.

Treatment groups

90 Participants
are divided into 1 treatment group
Group A: Digital health intervention groupExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Recruitment rate

Recruitment rate (n, %)

Time frame
From enrollment to end of the treatment at 8 weeks and the end of treatment at 6-month follow-up
2

Intervention adherence

Intervention adherence (n, %)

Time frame
From enrollment to end of the treatment at 8 weeks and the end of treatment at 6-month follow-up
3

Adverse events

Adverse events (n, %)

Time frame
From enrollment to end of the treatment at 8 weeks and the end of treatment at 6-month follow-up
4

Dropout rate

Dropout (n, %)

Time frame
From enrollment to end of the treatment at 8 weeks and the end of treatment at 6-month follow-up

Secondary outcomes

Other outcomes

Sponsors and contacts

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