Exercise Training in Asthma

NCT ID: NCT00820716

Last Updated: 2020-07-14

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

TERMINATED

Clinical Phase

NA

Total Enrollment

2 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-09-21

Study Completion Date

2010-10-15

Brief Summary

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The aim of the study is to compare two methods of exercise training: alternate load versus constant load realized at moderate or high intensities, in order to define the interests and the limits of each one of these two methods. The finality is to make possible to the expert to choose what exercise training induces the best results quickly and to make its choice according to the therapeutic objectives which it lays down.We also evaluate the effects of these exercises training on the vagal response and the bronchial tone of the asthmatics. From a clinical point of view, a close attention will be paid to the effects of these exercises training on the control of asthma and the quality of life of the subjects

Detailed Description

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Conditions

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Asthma

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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CA

Exercise training with alternate load

Group Type EXPERIMENTAL

Exercise training

Intervention Type OTHER

Comparison of two methods of exercise training: alternate load versus constant load realized at moderate or high intensities

CC

Exercise training with constant load

Group Type ACTIVE_COMPARATOR

Exercise training

Intervention Type OTHER

Comparison of two methods of exercise training: alternate load versus constant load realized at moderate or high intensities

Interventions

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Exercise training

Comparison of two methods of exercise training: alternate load versus constant load realized at moderate or high intensities

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* 18 to 45 years old
* mild to moderate persistent asthma (GINA classification)
* stabilized asthma
* physical activity level between 5 and 11 (Baecke and coll, 1982)
* no contra-indication for physical training

Exclusion Criteria

* cardiovascular pathology
* metabolic pathology
* traumatic pathology
* BMI≥30
* tobacco
* diabetes
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Strasbourg, France

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Evelyne LONSDORFER, MD

Role: STUDY_DIRECTOR

Hôpitaux Universitaires de Strasbourg

Locations

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Service de Physiologie et d'Explorations Fonctionnelles - Pôle de Pathologie Thoracique - Nouvel Hôpital Civil

Strasbourg, , France

Site Status

Service de Pneumologie - Pôle de Pathologie Thoracique - Nouvel Hôpital Civil

Strasbourg, , France

Site Status

Countries

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France

Other Identifiers

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2006-A00090-51

Identifier Type: -

Identifier Source: secondary_id

3825

Identifier Type: -

Identifier Source: org_study_id

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