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

Sponsor

University of Pennsylvania (Other)

Overall Status

Completed

CT.gov ID

NCT02080533

Collaborator

(none)

Enrollment

Location

Arm

24.9

Duration (Months)

0.4

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

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.

Condition or Disease	Intervention/Treatment	Phase
Pulmonary Arterial Hypertension	Other: Slow-paced respiration therapy	Phase 1/Phase 2

Study Design

Study Type:

Interventional

Actual Enrollment :

10 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

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

Study Start Date :

Feb 1, 2014

Actual Primary Completion Date :

Mar 1, 2015

Actual Study Completion Date :

Mar 1, 2016

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Single Slow-paced respiration therapy	Other: Slow-paced respiration therapy 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.

Arm

Intervention/Treatment

Experimental: Single

Slow-paced respiration therapy

Other: Slow-paced respiration therapy

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.

Outcome Measures

Primary Outcome Measures

Adherence to slow-paced respiration therapy. [10 weeks]
Adherence rates will be assessed by the frequency of days used.

Secondary Outcome Measures

Change in baseline and Week 10 dyspnea scores on the Multidimensional Dyspnea Profile [Baseline and 10 weeks]
Change in baseline and Week 10 fatigue scores on the Multidimensional Fatigue Inventory [Baseline and 10 weeks]
Change in baseline and Week 10 sleep scores on the Pittsburgh Sleep Quality Index [Baseline and 10 weeks]
Change in baseline and Week 10 norepinephrine levels [Baseline and 10 weeks]
Change in baseline and Week 10 interleukin-6 levels [Baseline and 10 weeks]
Change in baseline and Week 10 tumor necrosis factor-alpha levels [Baseline and 10 weeks]
Change in baseline and Week 10 six minute walk test [Baseline and 10 weeks]
Change in baseline and Week 10 right ventricular systolic pressure [Baseline and 10 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:

21 Years and Older

Sexes Eligible for Study:

Female

Accepts Healthy Volunteers:

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