Advanced Lung Disease Clinical Trial
— PREHABOfficial title:
Pilot Study of a Home-based Exercise Intervention to Treat Frailty in Lung Transplant Candidates
Verified date | March 2024 |
Source | University of California, San Francisco |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
In this pilot project, 35 lung transplant candidates will be recruited to participate in a three month individualized home-based program focused on exercise and nutrition optimization. This pilot is designed to assess the feasibility of treating frailty before lung transplantation. Participants will complete a 1 day in-person assessment and training session that will include baseline frailty assessment, determination of exercise capacity, and a determination of nutritional status. Based on American Thoracic Society Guidelines and a diet evaluation by a registered dietician, information gathered during the assessment will be used to develop a tailored prescription for exercise and nutrition to be continued at home. Participants will also be taught self-management skills specific to control of dyspnea, fatigue, motivation, and support. Participants will receive training in protocol implementation at home by a coordinator trained in principles of behavior change, adult learning theory, and dyspnea control techniques. Subjects will be provided tablet computers with an app called Aidcube preloaded and taught how to interface with the app. Aidcube is a commercially available exercise platform designed for patients with lung and heart diseases. It was designed with the input of physicians, physical therapists, respiratory therapists, nutritionists who specialize in patients with lung and heart disease and adheres to professional society guidelines for exercise and rehabilitation in patients with lung disease. Subjects will then adhere to a individually tailored home exercise and nutrition program based on their exercise capacity. Aidcube allows clinicians (or in this case the PI and co-PI) the ability to design a customized program of exercises and diet plan through the "provider interface". The subjects interacts with the "patient interface" to complete their exercise program during the 8 week study intervention. This goal of this pilot project is to determine the feasibility of implementing a home-based exercise and nutrition program with patients with advanced lung disease awaiting lung transplantation. Information on Aidcube can be found at https://www.aidcube.com. The overarching aim of this pilot study is preparatory investigation to evaluate the feasibility of performing a home-based intervention to treat frailty in lung transplant candidates. Specific aims: - Establish a sampling time frame and recruitment techniques. - Assess willingness to participate - Assess adherence and compliance. - Identify logistical problems in the in-person and at-home components of the intervention - Determine the resources needed for a full-scale study. - Provide funding bodies evidence that research team is competent and knowledgeable. - Provide funding bodies that the study is feasible
Status | Completed |
Enrollment | 26 |
Est. completion date | December 14, 2017 |
Est. primary completion date | December 14, 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 50 Years and older |
Eligibility | Inclusion Criteria: 1. Adult lung transplant candidates in the UCSF Lung Transplant Program aged >=50 2. Ability to understand and speak English or lives with a family member who has the ability to understand and speak English. 3. A diagnosis of chronic obstructive pulmonary disease (COPD) or pulmonary fibrosis (PF). 4. A supplemental oxygen requirement with exercise that can be delivered safely at home using their home oxygen concentrator (as determined by clinically available six-minute walk distance test) 5. Waitilisted or soon to be waitlisted for lung transplantation at UCSF 6. Short Physical Performance Battery (SPBB) frailty score of 9 or less (range 0 - 12; lower scores = worse frailty). 7. Must be an outpatient. 8. Willing and able to come to UCSF Parnassus Campus for 1 day in-person training program. Exclusion Criteria: 1. Inability to speak or understand English or does not live with a family member who has the abilty to understand and speak English. 2. Subject does not possess home oxygen equipment (if supplemental oxygen is required for exercise) 3. Already or soon to be enrolled in a traditional hospital based pulmonary rehabilitation program 4. Lives alone. 5. A diagnosis of primary or secondary pulmonary hypertension. Diagnosis will be determined by clinically available right heart catheterization pulmonary arterial mean pressure >= 30 mm Hg or transthoracic echocardiogram pulmonary arterial systolic pressure > 50 mm Hg or report of moderate right ventricular dysfunction or worse. These tests are performed as part of routine clinical care in the lung transplant program. Echocardiograms are repeated every 6 months while patients are listed for transplantation. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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University of California, San Francisco |
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* Note: There are 23 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Subject enrollment | Target patients who do not have access to traditional pulmonary rehabilitation programs | Through study completion, an average of 8 to 12 weeks | |
Primary | Subject attrition | Participant ability to complete program before receiving a lung transplant | Through study completion, an average of 8 to 12 weeks | |
Primary | Safety | Record number of adverse events, specifically (1) extreme breathlessness, fatigue, and/or weakness, (2) chest pain, (3) severe muscle pain, (4) dizziness or feeling faint, (5) leg pain, weakness or cramping, (6) sweating more than usual, (7) increase in mucus production, and (8) oxygen saturation levels falling below 85% during exercise | Through study completion, an average of 8 to 12 weeks | |
Secondary | Short Physical Performance Battery (SPPB) | Change in SPPB score (MCID = 1 point) | Pre-intervention at week 0 and post-intervention at week 8 | |
Secondary | Six Minute Walk Distance (6MWD) | Change in 6MWD (MCID = 30 meters | Pre-intervention at week 0 and post-intervention at week 8 |
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