Digital Follow-up Program for People with Chronic Obstructive Pulmonary Disease in Primary Healthcare
- Conditions
- COPD Chronic Obstructive Pulmonary Disease
- Interventions
- Behavioral: Guided self-determination (GSD) follow-up approach by primary care nurses.
- Registration Number
- NCT06401512
- Lead Sponsor
- Western Norway University of Applied Sciences
- Brief Summary
Chronic Obstructive Pulmonary Disease (COPD), characterized by non-reversible airflow obstruction, contributes to high mortality and morbidity rates worldwide, including Norway. Individuals with COPD experience symptoms and complications that impede daily activities and diminish their quality of life. COPD places a growing burden on healthcare systems presently and in the future. Interventions to empower individuals to self-manage their health effectively are needed to help the challenges of living with COPD, and work towards a sustainable healthcare system. As part of the broader healthcare policy agenda, this project aligns with the increasing emphasis on digital homebased primary healthcare. The intervention in this study will combine digital homebased care and guided self-determination follow-ups (GSD) within a general practice setting.
This project consists of 1) explore the feasibility of a COPD specific GSD counselling program delivered within a digital platform in primary care, 2) explore patients' and nurses' experiences applying the program, 3) examine the treatment fidelity of the intervention amongst healthcare professionals.
This project is a pilot cluster-randomized controlled trial (RCT), including individuals diagnosed with COPD, conducted in primary healthcare settings, and assessment of feasibility and uncertainties before conducting a later full-scale cluster-RCT. The intervention draws upon the Medical Research Council's revised guidelines for developing complex intervention studies, focusing on the initial phases of intervention development and pilot testing. Primary care clinics are randomly assigned into either an intervention- or a control group. The intervention consists of the GSD counselling program with follow-up within a digital platform. The control group provide regular care. The project will include both qualitative (individual semi-structured interviews), and quantitative data (questionnaires and clinical data).
In conclusion, this project explores an innovative intervention offering personalized strategies for COPD management in primary care clinic, by containing a digitalized homebased care program and follow-ups. The study aims to improve the daily living for people with COPD, while contributing to the future sustainability of healthcare systems.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 80
- Diagnosed with COPD living at home
- Post-bronchodilator forced expiratory volume 1 s (FEV1) to forced vital capacity (FVC) below lower limit of normality
- Severe somatic disease
- Severe psychiatric diagnosis
- Not able to provide informed consent
- Do not write, speak or understand Norwegian
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Intervention group Guided self-determination (GSD) follow-up approach by primary care nurses. -
- Primary Outcome Measures
Name Time Method Medical journal Baseline, and 3, 6, 9 and 12 months COPD-related information from medical journal
Questionnaire Baseline, and 3, 6, 9 and 12 months Patient satisfaction using Client Satisfaction Questionnaire (CSQ-8) and Patient global impression of change.
Weight Baseline and 12 months Weight in kg
Height Baseline and 12 months Height in cm
Recruitment rate for primary care practices Baseline Recruitment for primary care practices will be reported in terms of the number and proportion of primary care practices approached versus the practices that responded and, thereafter, the number who agreed to participate.
Qualitative data 6 - 18 months from baseline Individual interviews with participants
Recruitment rate for participants Baseline Participant recruitment will be reported in terms of the number of participants screened, found eligible, contacted, and those who provided written consent. Data for each recruitment step will be collected from all involved practices through self-reported numbers and the signed consent forms. Proportions will also be calculated for the number of participants screened versus those contacted, as well as for those contacted versus those who provided written consent.
Retention rate Baseline, and 3, 6, 9 and 12 months Retention will be reported as the number and proportion of participants who remain in the program at a certain timepoint. This will be calculated as the number of participants remaining in the program at each time point versus the number at baseline. To measure the retention rate, data from nurse reports, checklists, and medical records will be utilized.
Attrition rate Baseline, and 3, 6, 9 and 12 months The attrition rate, defined as the number of participants lost to follow-up, will be calculated as 1 minus the retention rate and as the number of participants lost to follow-up between consecutive time points. To measure the attrition rate, data from nurse reports, checklists, and medical records will be utilized. Additionally, data on who exited the program at what step and from whom we lack follow-up data will be collected.
Adherence rate Baseline, and 3, 6, and 9 months. Adherence rate will be collected in terms of number of sessions attended by each participant. To measure the adherence rate checklists and medical journals filled out by nurses conducting the intervention and self-reported data will be used.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Western Norway University of Applied Sciences
🇳🇴Bergen, Norway