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NCT07277855Active, not recruiting

Floor-Lift Series Pulmonary Rehabilitation for COPD: Short- and Long-Term Outcomes in a North African Setting

Evaluation of the Floor-Lift Series (FLS) Pulmonary Rehabilitation Program on Short- and Long-Term Clinical and Functional Outcomes in COPD by Program Adherence: A Single-Center Quasi-Experimental Study in a North African Setting

Source: ClinicalTrials.gov · Last updated 11 Dec 2025

Brief summary (registry, in English)

Chronic Obstructive Pulmonary Disease (COPD) is a major cause of morbidity and functional disability, with pulmonary rehabilitation (PR) representing one of the most effective non-pharmacological interventions. However, access to conventional PR programs remains extremely limited in many regions, particularly in North Africa, where resources, infrastructure, and patient adherence pose major challenges. The Floor-Lift Series (FLS) program was developed as a culturally adapted, equipment-free, and low-cost PR alternative. It is based on progressive floor-to-stand transitions - movements deeply integrated into daily routines and familiar in the local cultural context - to enhance feasibility and adherence. This prospective quasi-experimental study will evaluate both the short-term and long-term effects of the FLS program in COPD patients with baseline muscle dysfunction limiting their ability to rise from the floor. The short-term phase involves a 9-week intervention combining supervised and home-based training in three progressive stages (initial, intermediate, and consolidation). The long-term phase includes follow-up assessments at 18 months to evaluate sustained adherence and maintenance of clinical and functional improvements. The primary outcome is the completion rate, defined as achieving ≥22 daily floor-lift repetitions during the final intervention phase and maintaining adherence at long-term follow-ups. Secondary outcomes include changes in dyspnea (mMRC), exertional effort (Borg CR10), disease impact (CAT), mobility (Timed Up and Go), flexibility (fingertip-to-floor distance), exercise capacity (6-minute walk test and 1-minute sit-to-stand test), and the composite BODE index. Safety and psychosocial factors influencing adherence will be monitored throughout the study. The trial aims to provide evidence for a scalable, culturally relevant rehabilitation model for COPD management in resource-limited settings.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
16 (actual)
First submitted
19 Nov 2025
Start date
1 Dec 2024
Primary completion date
1 Dec 2026
Lead sponsor
Benazzouz Redouene Sid Ahmed
Diseases
COPD
NCT number
NCT07277855

What you commit to

  • Study type: Interventional
  • Participants enrolled: 16
  • From 1 Dec 2024 to the primary completion date, 1 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Acute COPD exacerbation or hospitalization within the previous 8 weeks.

Other illness

  • Recent myocardial infarction, unstable angina, or decompensated heart failure.
  • Severe neurological, orthopedic, or rheumatologic condition preventing safe floor exercise.
  • Cognitive impairment interfering with understanding or cooperation.

Other

  • Refusal or withdrawal of informed consent.

Who the study is looking for

  • Confirmed diagnosis of Chronic Obstructive Pulmonary Disease (COPD) according to GOLD 2023 criteria (post-bronchodilator FEV1/FVC \<0.7 and compatible clinical symptoms such as dyspnea or chronic cough) .
  • Presence of muscle dysfunction limiting or complicating the ability to rise from the floor.
  • Clinically stable condition (no COPD exacerbation within the past 8 weeks).
  • Provided written informed consent.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Laghouat University
Coordinator of this site? Confirm its status
LaghouatAlgeriaUnknown status

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This page is information, not medical advice. Discuss any trial with your doctor.