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Neuromuscular Electrical Stimulation in Patients With Interstitial Lung Disease

Effects of Neuromuscular Electrical Stimulation on Functional Exercise Capacity and Quality of Life in Patients With Interstitial Lung Disease

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02497144
Enrollment
30
Registered
2015-07-14
Start date
2015-07-15
Completion date
2018-12-30
Last updated
2022-04-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Interstitial Lung Disease

Keywords

interstitial lung disease, neuromuscular electrical stimulation, exercise capacity, quality of life

Brief summary

Decreased exercise capacity and quality of life, increased dyspnea and fatigue perception and hypoxemia during exercise is seen in patients with interstitial lung disease. Impaired ventilatory response, increased lung compliance, ventilation-perfusion mismatching and inadequate peripheral circulation causes decreased exercise capacity. Another important factor that induce decreased exercise capacity is peripheral muscle weakness. In literature, there is no study investigated effects of neuromuscular electrical stimulation on functional exercise capacity, respiratory and peripheral muscle strength, pulmonary functions, physical activity level, dyspnea and fatigue perception in patients with interstitial lung disease.

Detailed description

In literature, there was increased quantity of study investigated effects of neuromuscular electrical stimulation in chronic lung disease patients. It was used as a pulmonary rehabilitation component especially in patients with decreased exercise capacity and peripheral muscle strength, intensely increased dyspnea inhibits exercise. It was demonstrated that neuromuscular electrical stimulation improved functional exercise capacity, peripheral muscle strength and quality of life.

Interventions

Neuromuscular electrical stimulation

OTHERControl Group

Breathing exercises

Sponsors

Gazi University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosed with interstitial lung disease * Clinically stable * Under standard medication * Having no exacerbation or infection

Exclusion criteria

* Cognitive disorders * Orthopedic and neurological problems * Contraindications to apply the neuromuscular electrical stimulation (pace maker, sensory defects, etc...)

Design outcomes

Primary

MeasureTime frameDescription
Functional exercise capacity6 weeksSix minute walk test

Secondary

MeasureTime frameDescription
Inspiratory and expiratory muscle strength (MIP,MEP)6 weeksMouth pressure device
Dyspnea6 weeksModified Borg and Modified Medical Research Council (MMRC) Dyspnea scales
Peripheral muscle strength6 weeksHand held dynamometer
Maximal exercise capacity6 weeksIncremental shuttle walk test
Fatigue6 weeksFatigue Severity Scale
Pulmonary functions6 weeksSpirometry
Cough related quality of life6 weeksLeicester Cough Questionnaire
Depression6 weeksMontgomery Asberg Depression Rating Scale (MADRS) (Turkish versions of all scales)
Generic quality of life6 weeksShort Form (SF-36) Health Survey
Disease specific quality of life6 weeksSaint George Quality of Life Questionnaire
Physical activity6 weeksMetabolic holter

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026