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The Effect of Distractive Auditory Stimuli (Music) on Dyspnea and Anxiety During Exercise in Adults With Chronic Respiratory Diseases

NYU Langone Health logo

NYU Langone Health

Status

Completed

Conditions

Chronic Obstructive Pulmonary Disease

Treatments

Procedure: Distractive Auditory Stimuli
Procedure: No Distractive Auditory Stimuli

Study type

Interventional

Funder types

Other

Identifiers

NCT02955108
16-01676

Details and patient eligibility

About

The objective of this study is to look at the effects of distractive auditory stimuli (DAS) on reducing dyspnea intensity and related anxiety and increasing exercise tolerance. Investigators hope that compared to a no-music control condition, that under a music condition participants with COPD will (a) demonstrate increased self-paced walk distance and enjoyment; (b) have less dyspnea intensity, (c) experience less dyspnea anxiety; (d) have less fatigue and state anxiety; and (e) higher maximum heart rate. The upbeat music with a tempo of 90 - 100 bpm (an average-to-moderate walking tempo) is expected to have distractive and performance enhancing effects in order to increase tolerance to dyspnea and exercise. The long-term goal of this study is to increase physical activity in adults with COPD and RLD by promoting dyspnea and fatigue management through use of distractive auditory stimuli in the form of music.

Full description

This randomized clinical trial will use a cross-over design. The research will include two within-subject factors, music versus no music and time. Each subject will be randomized a single time to receive either music first then no music, or alternatively, no music first then music during two walk tests.

Enrollment

8 patients

Sex

All

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • English speaking

  • aged 40 years or older, with physician-diagnosed COPD

  • a flow volume loop with a FEV1/FVC of < 0.70 in the past 12 months

    • medically cleared to participate in NYULMC's pulmonary rehabilitation program.

Exclusion criteria

  • Inability to exercise due to musculoskeletalor neurological dysfunction
  • Inability to walk independently (unaided)
  • deafness or severe hearing impairment requiring hearing aids
  • mMRC score = 0 ("I only get breathlessness with strenuous exercise").

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

8 participants in 2 patient groups

music first then no music
Experimental group
Treatment:
Procedure: Distractive Auditory Stimuli
Procedure: No Distractive Auditory Stimuli
no music first then music
Experimental group
Treatment:
Procedure: Distractive Auditory Stimuli
Procedure: No Distractive Auditory Stimuli

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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