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OpenTrials
Completed

NCT Number: NCT04745000

Observational Study of Actigraphy in Pediatric Pulmonary Arterial Hypertension

This study plans to learn more about activity levels in children with pulmonary hypertension. Pulmonary hypertension is a condition where the pressure in the lungs is higher than normal. This can affect the person's heart. The purpose of this study is to see if measuring activity in children with pulmonary hypertension and comparing it to activity in children without pulmonary hypertension can give their doctor helpful information on how they are feeling and how their treatment is working.

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Key information

Age range

Up to 6 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Children's Hospital Colorado

Aurora, Colorado, 80045, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

for children with PAH:

  • Ages 0-6 years at the time of consent
  • Current diagnosis of pulmonary hypertension in World Health Organization (WHO) Diagnostic Group 1 as per established clinical criteria including prior catheterization meeting Group 1 criteria
  • Panama Functional Class II-IIIa
  • Must have been receiving an approved oral endothelin receptor antagonist, calcium channel blocker, phosphodiesterase 5 inhibitor, prostanoid and/or soluble guanylate cyclase stimulator for at least 30 days prior to consent, and has been at the current stable dose, other than weight-based adjustments, for at least 30 days prior to consent
  • On stable doses of other medical therapy for 14 days prior to enrollment visit with no dose adjustments, additions, or discontinuations (exception diuretics and anticoagulants; OTC/cold/seasonal allergy medications).

Exclusion criteria

for children with PAH:

  • Diagnosis of congenital diaphragmatic hernia, or a chronic lung disease, such as bronchopulmonary dysplasia, or interstitial lung disease
  • Any bone (e.g., osteogenesis imperfecta, ankle, knee, or hip injuries), neuromuscular (e.g., muscular dystrophy), or other pathology that may limit activity (e.g., arthritis)
  • Down syndrome
  • Use of any medications known to limit activity (e.g., sedative)
  • Active infection (may re-screen for enrollment once resolved)
  • Any other cardiovascular, liver, renal, hematologic, gastrointestinal, immunologic, endocrine, metabolic, or central nervous system disease or condition that, in the opinion of the Investigator, may adversely affect the safety of the participant or interfere with the interpretation of study assessments

Examples:

  • Current diagnosis of uncontrolled sleep apnea as defined by their physician
  • Severe renal insufficiency as defined by the requirement for dialysis at screening
  • Moderate to severe hepatic dysfunction defined as elevated aspartate aminotransferase (AST) or alanine aminotransferase (ALT) liver function tests, greater than or equal to three times the upper limit of normal at screening
  • Actively listed for transplantation
  • Patient and/or legal guardian has/have an unstable psychiatric condition or is/are mentally incapable of understanding the objectives, nature, or consequences of the trial, or has any condition in which the Investigator's opinion would constitute an unacceptable risk to the participant's safety

Inclusion criteria

for control children:

  • Ages 0-6 years at the time of consent
  • In good general health as evidenced by medical history reported by parent/legal guardian during screening and/or available medical records

Exclusion criteria

for control children:

  • Known diagnosis of asthma (controlled or uncontrolled)
  • Inability to exercise normally either due to an intellectual disability (e.g., Down Syndrome), or a physical disability which could impede activities of daily living.
  • Child and/or legal guardian has/have an unstable psychiatric condition or is/are mentally incapable of understanding the objectives, nature, or consequences of the trial, or has any condition in which the Investigator's opinion would constitute an unacceptable risk to the participant's safety

Treatment and study plan

Primary outcomes

  1. Number of Participants Meeting Compliance threshold for wearing actigraphy devices: Visit 1

    Time frame: Over 14 Days, reported at Day 15 post baseline (Visit 1)

    Actigraphy device wear compliance threshold is a minimum of 4 hours per day, and 8 compliant days out of 14 days of wear time.

  2. Number of Participants Meeting Compliance threshold for wearing actigraphy devices: Visit 2

    Time frame: Over 14 days, reported at about 6 months post-baseline (Visit 2)

    Actigraphy device wear compliance threshold is a minimum of 4 hours per day, and 8 compliant days out of 14 days of wear time.

  3. Number of skin irritation adverse events: Visit 1

    Time frame: Over 14 Days, reported at Day 15 post baseline (Visit 1)

  4. Number of skin irritation adverse events: Visit 2

    Time frame: Over 14 days, reported at about 6 months post-baseline (Visit 2)

Secondary outcomes

  1. Heart rate: Visit 1

    Time frame: Over 14 Days, reported at Day 15 post baseline (Visit 1)

    Measured via Fitbit.

  2. Heart rate: Visit 2

    Time frame: Over 14 days, reported at about 6 months post-baseline (Visit 2)

    Measured via Fitbit.

  3. Steps per day: Visit 1

    Time frame: Over 14 Days, reported at Day 15 post baseline (Visit 1)

    Measured via Fitbit and ActiGraph wGT3x-BT.

  4. Steps per day: Visit 2

    Time frame: Over 14 days, reported at about 6 months post-baseline (Visit 2)

    Measured via Fitbit and ActiGraph wGT3x-BT.

  5. Miles per day: Visit 1

    Time frame: Over 14 Days, reported at Day 15 post baseline (Visit 1)

    Measured via Fitbit.

  6. Miles per day: Visit 2

    Time frame: Over 14 days, reported at about 6 months post-baseline (Visit 2)

    Measured via Fitbit.

  7. Energy expenditure per day (kcal): Visit 1

    Time frame: Over 14 Days, reported at Day 15 post baseline (Visit 1)

    Measured via Fitbit and ActiGraph wGT3x-BT.

  8. Energy expenditure per day (kcal): Visit 2

    Time frame: Over 14 days, reported at about 6 months post-baseline (Visit 2)

    Measured via Fitbit and ActiGraph wGT3x-BT.

  9. Active minutes per day: Visit 1

    Time frame: Over 14 Days, reported at Day 15 post baseline (Visit 1)

    Measured via Fitbit.

  10. Active minutes per day: Visit 2

    Time frame: Over 14 days, reported at about 6 months post-baseline (Visit 2)

    Measured via Fitbit.

  11. Count of Activity Bouts: Visit 1

    Time frame: Over 14 Days, reported at Day 15 post baseline (Visit 1)

    Count of Active bouts recorded and defined by the Actigraphy devices.

  12. Count of Activity Bouts: Visit 2

    Time frame: Over 14 days, reported at about 6 months post-baseline (Visit 2)

    Count of Active bouts recorded and defined by the Actigraphy devices.

  13. Count of Sedentary Bouts: Visit 1

    Time frame: Over 14 Days, reported at Day 15 post baseline (Visit 1)

    Count of Sedentary Bouts recorded and defined by the Actigraphy devices.

  14. Count of Sedentary Bouts: Visit 2

    Time frame: Over 14 days, reported at about 6 months post-baseline (Visit 2)

    Count of Sedentary Bouts recorded and defined by the Actigraphy devices.

  15. Activity Count: Visit 1

    Time frame: Over 14 Days, reported at Day 15 post baseline (Visit 1)

    Count of Activity Events recorded and defined by the Actigraphy devices.

  16. Activity Count: Visit 2

    Time frame: Over 14 days, reported at about 6 months post-baseline (Visit 2)

    Count of Activity Events recorded and defined by the Actigraphy devices.

  17. Physical Activity intensity: Visit 1

    Time frame: Over 14 Days, reported at Day 15 post baseline (Visit 1)

    Number of minutes with "Mild", "Moderate", and "Vigorous" physical activity.

  18. Physical Activity intensity: Visit 1

    Time frame: Over 14 days, reported at about 6 months post-baseline (Visit 2)

    Number of minutes with "Mild", "Moderate", and "Vigorous" physical activity.

  19. Resting oxygen saturation at Baseline

    Time frame: Baseline

  20. Resting oxygen saturation at Visit 2

    Time frame: About 6 months post baseline

  21. Number of PH Participants with Clinical Worsening (CW) Events

    Time frame: End of Study (Up to 12 months post baseline)

  22. Number of PH Participants with Genetic Mutations or Positive Genetic tests

    Time frame: End of Study (Up to 12 months post baseline)

    Count of PH participants with an observed positive genetic test or genetic mutation.

  23. Natriuretic Peptide Tests - BNP

    Time frame: End of Study (Up to 12 months post baseline)

    Brain natriuretic peptide (BNP): a heart failure marker

  24. Natriuretic Peptide Tests - NT-proBNP)

    Time frame: End of Study (Up to 12 months post baseline)

    N-terminal pro b-type natriuretic peptide (NT-proBNP): a heart failure marker

Sponsors and collaborators

Lead sponsor

University of Colorado, Denver

Other

Collaborators

  • Children's Hospital Colorado
  • Food and Drug Administration (FDA)

Registry information

Official study title

A Prospective Study to Investigate the Use of Actigraphy as a Novel, Reliable and Non-invasive Study Endpoint to Facilitate Pediatric Pulmonary Arterial Hypertension Trials and Drug Development for Children Ages 0-6 Years

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Feb 9, 2021
Registry last updated
May 10, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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