Effect of Different Form of Upper Limb Muscles Training on Dyspnea in COPD

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

280 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-11-21

Study Completion Date

2023-02-06

Brief Summary

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Evaluate the effect of upper limbs strength training versus the effect of upper limbs endurance training, on dyspnea, in patients with COPD during a pulmonary rehabilitation program.

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Detailed Description

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Conditions

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COPD

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

This is a multicenter, prospective, randomized, open-label study.

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Strength

Patients will follow the pulmonary rehabilitation program associated with upper limbs strength training for a duration of 4 weeks

Group Type EXPERIMENTAL

Strength training

Intervention Type OTHER

Upper limbs Strength training; done with dumbbells whose weight corresponds to 60-80% of the maximal voluntary force in abduction measured initially, during 4 weeks

Endurance

Patients will follow the pulmonary rehabilitation program associated with upper limbs endurance training for a duration of 4 weeks

Group Type ACTIVE_COMPARATOR

Endurance training

Intervention Type OTHER

Upper limbs Endurance training of the ; done with dumbbells whose weight corresponds to 30% of the maximum voluntary force in abduction measured initially, during 4 weeks

Interventions

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Strength training

Upper limbs Strength training; done with dumbbells whose weight corresponds to 60-80% of the maximal voluntary force in abduction measured initially, during 4 weeks

Intervention Type OTHER

Endurance training

Upper limbs Endurance training of the ; done with dumbbells whose weight corresponds to 30% of the maximum voluntary force in abduction measured initially, during 4 weeks

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patient with stage 2 to 4 (A to D) COPD admitted to a pulmonary rehabilitation program (4 weeks)
* Patient aged 18 or over
* Patient able to consent and having signed a consent form

Exclusion Criteria

* Patient with pain, osteoarthritis or shoulder surgery
* Patient with a history of Pneumonectomy, lobectomy less than 6 months old
* Refusal of participation
* Patient with an inability to complete a pulmonary rehabilitation program in totality
* Pregnant or breast-feeding women
* Patient under tutorship or curatorship

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No