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Completed

NCT Number: NCT02080533

Feasibility of Slow-paced Respiration Therapy for Treatment of a Symptom Cluster in Pulmonary Arterial Hypertension

Pulmonary arterial hypertension (PAH) is a chronic illness characterized by increased pulmonary pressures resulting in right heart failure and premature death. Common symptoms that impair quality of life and functioning are dyspnea, fatigue and sleep disturbance. This trio of symptoms is highly prevalent and forms a symptom cluster (2 or more symptoms that co-occur) in PAH. From a biological, proinflammatory cytokines are implicated in dyspnea, fatigue and sleep disturbance; there is activation of the sympathetic nervous system (SNS) and an inherent inflammatory process in PAH that contributes to the pathophysiology, but the link to this symptom cluster has not been investigated. One novel, treatment for symptom clusters is slow-paced respiration therapy using the FDA-approved device, RESPeRATE. The device contains headphones and a sensor that attaches to the chest to detect inhalation and exhalation. Musical tones synchronize with the respiratory cycle to slowly guide the user to decrease respirations. RESPeRATE moderates effects of the SNS; lowers blood pressure; improves functional capacity and ejection fraction; and significantly decreases pulmonary pressures in left heart failure. The investigators will enroll 10 women with PAH to use the RESPeRATE device to perform slow-paced respiration for 15 minutes per day for 8 weeks to determine the feasibility and effects on the SNS and inflammatory activity and the symptom cluster. The investigator's overall hypothesis is that, as compared to baseline, after eight weeks of therapy women with PAH who receive slow-based respiration therapy will have lower SNS activity and inflammatory levels, and improved dyspnea, fatigue and sleep disturbance.

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Key information

Age range

21 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

University of Pennsylvania

Philadelphia, Pennsylvania, 19104, United States

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Previous documentation of mean pulmonary artery pressure > 25 mm Hg with a pulmonary capillary wedge pressure (or left ventricular end-diastolic pressure) < 16 mm Hg and PVR > 3 WU at any time before study entry.
  • Women with WHO Group I PAH (idiopathic, heritable, or associated with connective tissue disease, congenital heart disease, anorexigens or HIV)
  • Targeted PAH therapy at stable dose for 3 months
  • Age >21 years
  • Ability to perform six minute walk testing without limitations in musculoskeletal function or coordination.
  • Informed consent

Exclusion criteria

  • Age < 21
  • Hypotension (blood pressure < 90/60 mmHg)
  • Pregnancy
  • Chronic Fatigue Syndrome (current or history of)
  • Known sleep disorder (obstructive sleep apnea, restless leg syndrome, narcolepsy, current or history of)
  • Hospitalized or acutely ill
  • Major Depression (current or history of)
  • Lung transplant recipient

Treatment and study plan

Slow-paced respiration therapy

Other

The FDA-approved RESPeRATE device contains headphones and a sensor that attaches to the chest to detect inhalation and exhalation. Musical tones synchronize with the respiratory cycle to slowly guide the user to decrease respirations.

Primary outcomes

  1. Adherence to slow-paced respiration therapy.

    Time frame: 10 weeks

    Adherence rates will be assessed by the frequency of days used.

Secondary outcomes

  1. Change in baseline and Week 10 dyspnea scores on the Multidimensional Dyspnea Profile

    Time frame: Baseline and 10 weeks

  2. Change in baseline and Week 10 fatigue scores on the Multidimensional Fatigue Inventory

    Time frame: Baseline and 10 weeks

  3. Change in baseline and Week 10 sleep scores on the Pittsburgh Sleep Quality Index

    Time frame: Baseline and 10 weeks

  4. Change in baseline and Week 10 norepinephrine levels

    Time frame: Baseline and 10 weeks

  5. Change in baseline and Week 10 interleukin-6 levels

    Time frame: Baseline and 10 weeks

  6. Change in baseline and Week 10 tumor necrosis factor-alpha levels

    Time frame: Baseline and 10 weeks

  7. Change in baseline and Week 10 six minute walk test

    Time frame: Baseline and 10 weeks

  8. Change in baseline and Week 10 right ventricular systolic pressure

    Time frame: Baseline and 10 weeks

Sponsors and collaborators

Lead sponsor

University of Pennsylvania

Other

Registry information

Important dates

Study start
2014
Primary completion
2015
Study completion
2016
First posted
Mar 6, 2014
Registry last updated
Aug 31, 2016

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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