Effects of Training in Healthy Sedentary Subjects
Cellular Effects of Training in Healthy Sedentary Subjects
1 other identifier
interventional
30
1 country
3
Brief Summary
The purpose of this study is to understand underlying mechanisms of improved exercise tolerance in Healthy Sedentary Subjects after training program.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started May 2008
Typical duration for not_applicable
3 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2008
CompletedFirst Submitted
Initial submission to the registry
August 16, 2010
CompletedFirst Posted
Study publicly available on registry
August 17, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2010
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2010
CompletedSeptember 5, 2012
September 1, 2012
2.6 years
August 16, 2010
September 3, 2012
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Effects of training program on mitochondrial function and oxidative stress
6 to 8 weeks
Secondary Outcomes (1)
Relationship between mitochondrial function, oxidative stress and exercise tolerance in COPD patients
6 to 8 weeks
Study Arms (2)
Ventilatory threshold
ACTIVE COMPARATORTraining at the ventilatory threshold
Metabolic threshold
ACTIVE COMPARATORTraining at the metabolic threshold
Interventions
Eligibility Criteria
You may qualify if:
- healthy Sedentary Subjects
You may not qualify if:
- neuromuscular disease
- chronic heart failure
- diabetes
- renal diseases
- liver diseases
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (3)
Clinique du souffle La valonie
Lodève, France
hopital Arnaud de Vilneuve
Montpellier, France
Clinique du souffle La solane
Osséja, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Maurice MH Hayot, MCU-PH
Institut National de la Santé Et de la Recherche Médicale, France
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 16, 2010
First Posted
August 17, 2010
Study Start
May 1, 2008
Primary Completion
December 1, 2010
Study Completion
December 1, 2010
Last Updated
September 5, 2012
Record last verified: 2012-09