NCT01183052

Brief Summary

The purpose of this study is to understand the underlying mechanisms of improved exercise tolerance in COPD patients after training program.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jun 2009

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2009

Completed
1.2 years until next milestone

First Submitted

Initial submission to the registry

August 16, 2010

Completed
1 day until next milestone

First Posted

Study publicly available on registry

August 17, 2010

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2010

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2010

Completed
Last Updated

September 5, 2012

Status Verified

September 1, 2012

Enrollment Period

1.5 years

First QC Date

August 16, 2010

Last Update Submit

September 3, 2012

Conditions

COPD Patients

Keywords

COPDexercise toleranceoxidative stress

Outcome Measures

Primary Outcomes (1)

  • Cellular effects of exercise training at the ventilatory threshold intensity

    6 to 8 weeks

Study Arms (1)

Training

OTHER

20 sessions of training

Other: Training

Interventions

TrainingOTHER

20 sessions of training

Also known as: CT
Training

Eligibility Criteria

Age50 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Sedentary mild to severe COPD patients

You may not qualify if:

  • Neuromuscular disease
  • Chronic heart failure
  • Renal diseases
  • Liver diseases
  • Obesity

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Clinique du Souffle La Vallonie

Lodève, 34700, France

Location

Clinique du Souffle la Solane

Osséja, 66340, France

Location

MeSH Terms

Conditions

Pulmonary Disease, Chronic Obstructive

Condition Hierarchy (Ancestors)

Lung Diseases, ObstructiveLung DiseasesRespiratory Tract DiseasesChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Maurice MH Hayot, MCU-PH

    Institut National de la Santé Et de la Recherche Médicale, France

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 16, 2010

First Posted

August 17, 2010

Study Start

June 1, 2009

Primary Completion

December 1, 2010

Study Completion

December 1, 2010

Last Updated

September 5, 2012

Record last verified: 2012-09

Locations

FR(2)