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Physical Activity in Pediatric Pulmonary Hypertension (PedPH-XRcise)

Primary Purpose

Pulmonary Hypertension

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Exercise intervention
Sponsored by
Children's Hospital of Philadelphia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pulmonary Hypertension

Eligibility Criteria

8 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 8-18 years
  • PH World Health Organization (WHO) diagnostic groups 1, 2, or 3 (pulmonary arterial hypertension, PH due to left heart disease, PH due to lung disease)
  • WHO functional class I or II
  • Ambulatory status
  • Mean pulmonary to systemic arterial pressure ratio <0.75 on most recent cardiac catheterization
  • Oxygen saturation >85% on 6-minute walk test
  • Stable PH medication regimen for 3 months prior to the intervention,

Exclusion Criteria:

  • WHO functional class III or IV
  • Single ventricle physiology
  • Moderate to severe renal disease (>stage 3)
  • Severe hepatic impairment [aspartate aminotransferase (AST)/alanine transaminase (ALT) > 2x upper limit of normal]
  • Current pregnancy
  • Significant developmental delay/inability to comply with verbal instructions to complete the study procedures

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Other

    Arm Label

    Home exercise intervention

    Arm Description

    Participants will be instructed in performing aerobic exercise for 20 minutes per day, 5 days per week, and light resistance exercises 2 days per week. Aerobic sessions will start with stretching followed by walking, biking, or light jogging, depending on access to facilities/equipment and weather. Participants will increase their heart rate on the smartwatch to a goal of 80% that achieved on their 6-minute walk test (at most 150 beats/min). Participants will perform light resistance exercises using resistance bands. Participants will be advised to avoid heavy exercise. Participants will wear the smartwatch for the length of the intervention. This will synch with a mobile device application to support at-home symptom assessment, recording of resistance exercise, and protocol adherence. There will be multiple ways (videochat, telephone ChatBot) by which participants can contact the study team with questions or concerns.

    Outcomes

    Primary Outcome Measures

    Change in moderate to vigorous physical activity (MVPA)
    Change in MVPA (min/day) will be measured by accelerometer from baseline over the course of the intervention

    Secondary Outcome Measures

    Change in leg lean mass Z-score (LLMZ)
    LLMZ will be measured by densitometry. LLMZ is a percentile score with scores -2 to 2 considered typical
    Change in muscle strength
    Upper extremity strength will be measured by handgrip dynamometer. Lower extremity strength will be measured by Biodex across the knee and ankle
    Change in 6-minute walk test distance
    6-minute walk distance (in meters) will be measured per standard American Thoracic Society guidelines
    Change in quality of life score
    Score measured by completion of PedsQL questionnaire. Scores range from 0-100 with higher scores indicating better quality of life

    Full Information

    First Posted
    June 24, 2022
    Last Updated
    March 24, 2023
    Sponsor
    Children's Hospital of Philadelphia
    Collaborators
    National Heart, Lung, and Blood Institute (NHLBI)
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05442671
    Brief Title
    Physical Activity in Pediatric Pulmonary Hypertension
    Acronym
    PedPH-XRcise
    Official Title
    Understanding the Barriers to Physical Activity in Pediatric Pulmonary Hypertension in Order to Design Effective Home-based Exercise Programs
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    February 1, 2024 (Anticipated)
    Primary Completion Date
    March 1, 2026 (Anticipated)
    Study Completion Date
    March 1, 2026 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Children's Hospital of Philadelphia
    Collaborators
    National Heart, Lung, and Blood Institute (NHLBI)

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Children with pulmonary hypertension (PH) engage in less physical activity than their peers. This is a concern since adult data support exercise as a non-pharmacologic treatment for PH. Despite adult data, therapeutic exercise has not been widely adopted in pediatric PH. Investigators have previously demonstrated that children with PH have less skeletal muscle mass in association with worse exercise performance. Interventions to increase physical activity and skeletal muscle mass may improve exercise performance and quality of life in children with PH. This study will use wearable activity monitoring devices to promote physical activity in a 16-week pilot intervention in children and teenager with PH.
    Detailed Description
    Pediatric pulmonary hypertension (PH) is a rare disease, affecting 2-16 per million children. Without treatment, pulmonary vascular disease leads to right ventricular cardiac failure and death. Survival has improved with pharmacologic advances, however, 5-year survival from diagnosis is still only about 75%. Even with increased survival, pediatric PH is a severe, chronic illness with physical and psychosocial burdens affecting the quality of life of children and families. Exercise intolerance is nearly universal and adversely affects quality of life. While exercise physiology is complex, skeletal muscle deficits and dysfunction are important factors associated with exercise intolerance in adults with PH. The contraction of the skeletal muscle pump helps increase pulmonary blood flow at the initiation of upright exercise in the normal circulation. Low skeletal muscle mass and muscle dysfunction may impair this mechanism in PH. Investigators previously demonstrated low skeletal muscle mass in association with worse exercise performance in children with PH and identified this as an intervention target. As children with PH engage in less moderate and vigorous physical activity compared to healthy peers, we hypothesize that increasing physical activity could increase skeletal muscle mass and lead to improved exercise performance. Recent trials have demonstrated improved exercise performance and functional class in adults with PH undertaking prescribed exercise training. Pediatric data are limited to a single, small study in which exercise performance improved after a 16-week home exercise program. That intervention did not include skeletal muscle assessment, wearable activity monitors, or specified behavioral theory, as does the current proposal. The characteristics of the optimal PH exercise program are not clear as prior studies often failed to provide sufficient detail to enable reproducibility. Most programs have been hospital-based, some with additional at-home components. Duration has varied from 4-15 weeks. Programs have included aerobic, resistance, and respiratory exercise. Patient adherence has been inconsistently assessed. While wearable activity monitors have been used to assess activities of daily living of PH patients, they have not been employed in PH exercise programs. In youth, practical concerns of developmental differences, access to facilities or equipment, and parental time commitment must be considered, and home programs may be critical to avoiding missed school and work. Newer technologic advances enable remote monitoring of physical activity in the home setting. Wearable accelerometer sensors with wireless transmission capabilities allow us to measure relevant endpoints from a patient's daily life. In this study, participants will undergo baseline assessment of muscle mass and strength, 6-minute walk test distance, and quality of life prior to a 16-week home exercise program, enriched by mobile health technology. Investigators will use a wrist-worn accelerometer paired with a custom mobile device application on a smart device to measure activity, obtain daily downloads, and engage patients to promote adherence. Assessment of muscle mass and strength, 6-minute walk test distance, and quality of life will be repeated after the intervention. This real-time monitoring of adherence and feedback to the patient represent fundamental changes in PH treatment paradigms that can significantly enhance efficacy.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Pulmonary Hypertension

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    25 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Home exercise intervention
    Arm Type
    Other
    Arm Description
    Participants will be instructed in performing aerobic exercise for 20 minutes per day, 5 days per week, and light resistance exercises 2 days per week. Aerobic sessions will start with stretching followed by walking, biking, or light jogging, depending on access to facilities/equipment and weather. Participants will increase their heart rate on the smartwatch to a goal of 80% that achieved on their 6-minute walk test (at most 150 beats/min). Participants will perform light resistance exercises using resistance bands. Participants will be advised to avoid heavy exercise. Participants will wear the smartwatch for the length of the intervention. This will synch with a mobile device application to support at-home symptom assessment, recording of resistance exercise, and protocol adherence. There will be multiple ways (videochat, telephone ChatBot) by which participants can contact the study team with questions or concerns.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Exercise intervention
    Intervention Description
    16-week home exercise intervention, enriched by mobile health technology
    Primary Outcome Measure Information:
    Title
    Change in moderate to vigorous physical activity (MVPA)
    Description
    Change in MVPA (min/day) will be measured by accelerometer from baseline over the course of the intervention
    Time Frame
    Pre-exercise intervention and Post intervention (within 2 weeks of completion of the 16-week exercise intervention)
    Secondary Outcome Measure Information:
    Title
    Change in leg lean mass Z-score (LLMZ)
    Description
    LLMZ will be measured by densitometry. LLMZ is a percentile score with scores -2 to 2 considered typical
    Time Frame
    Pre-exercise intervention and Post intervention (within 2 weeks of completion of the 16-week exercise intervention)
    Title
    Change in muscle strength
    Description
    Upper extremity strength will be measured by handgrip dynamometer. Lower extremity strength will be measured by Biodex across the knee and ankle
    Time Frame
    Pre-exercise intervention and Post intervention (within 2 weeks of completion of the 16-week exercise intervention)
    Title
    Change in 6-minute walk test distance
    Description
    6-minute walk distance (in meters) will be measured per standard American Thoracic Society guidelines
    Time Frame
    Pre-exercise intervention and Post intervention (within 2 weeks of completion of the 16-week exercise intervention)
    Title
    Change in quality of life score
    Description
    Score measured by completion of PedsQL questionnaire. Scores range from 0-100 with higher scores indicating better quality of life
    Time Frame
    Pre-exercise intervention and Post intervention (within 2 weeks of completion of the 16-week exercise intervention)

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    8 Years
    Maximum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Age 8-18 years PH World Health Organization (WHO) diagnostic groups 1, 2, or 3 (pulmonary arterial hypertension, PH due to left heart disease, PH due to lung disease) WHO functional class I or II Ambulatory status Mean pulmonary to systemic arterial pressure ratio <0.75 on most recent cardiac catheterization Oxygen saturation >85% on 6-minute walk test Stable PH medication regimen for 3 months prior to the intervention, Exclusion Criteria: WHO functional class III or IV Single ventricle physiology Moderate to severe renal disease (>stage 3) Severe hepatic impairment [aspartate aminotransferase (AST)/alanine transaminase (ALT) > 2x upper limit of normal] Current pregnancy Significant developmental delay/inability to comply with verbal instructions to complete the study procedures

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

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