Examining the Effects of a Remote Pulmonary Rehabilitation Program in the Severe Asthma Population.
- Conditions
- Asthma
- Interventions
- Behavioral: Pulmonary rehab programBehavioral: Placebo
- Registration Number
- NCT06150300
- Lead Sponsor
- University of Saskatchewan
- Brief Summary
This is a randomized control trial evaluating the effect of a novel mobile application-delivered pulmonary rehabilitation program in adult severe asthma patients. The intervention will include eight weeks of exercise videos that progress in difficulty, as well as asthma-specific educational content. The primary outcome measure is change in functional exercise capacity as measured by six-minute walk distance. Secondary outcome measures will include evaluation of overall feasibility, and change in CPET parameters such as VO2max. Change in asthma control questionnaire (ACQ), asthma quality of life questionnaire (AQLQ) and PRAISE self-efficacy score will also be evaluated.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 34
- Adults aged 18 years and older with a diagnosis of asthma by a respirologist. They must have severe disease defined by GINA severity classification. Participants must have access to a smartphone or internet browser to allow access to study content.
- Exclusion criteria include comorbid cardiopulmonary or musculoskeletal conditions that may impact exercise tolerance in accordance with the American Thoracic Society CPET guidelines
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Physical activity intervention Pulmonary rehab program 8 week virtual pulmonary rehab program including breathing exercises and educational messages. Placebo Placebo Breathing exercises and educational messages
- Primary Outcome Measures
Name Time Method CPET After 8 weeks of intervention VO2max
- Secondary Outcome Measures
Name Time Method