Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
28 participants
INTERVENTIONAL
2019-01-01
2019-04-27
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
ET
Active Comparator: ET Endurance training were prformed. Intensity was gradually increased.
Endurance Training ET
Endurance training were prformed. Intensity was gradually increased.
RT
Resistance training were prformed. Intensity was gradually increased.
Resistance Training RT
Resistance training were prformed. Intensity was gradually increased.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Endurance Training ET
Endurance training were prformed. Intensity was gradually increased.
Resistance Training RT
Resistance training were prformed. Intensity was gradually increased.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Clinically stable
* Abscence of other obstructive diseases
* Signed written consent
Exclusion Criteria
* cardiovascular diseases.
* Contre-indications to physical therapy
* Acute exacerbations a month before the intervention
40 Years
75 Years
MALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Faculty of Medicine, Sousse
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Acheche Amal
PhD student
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Amal Acheche, Phd
Role: PRINCIPAL_INVESTIGATOR
Faculty of Medicine of Sousse Sousse, Tunisia
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Amal Acheche
Sousse, , Tunisia
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
authors non mentionned., global initiative for chronic lung disease. 2017
Molfino NA, Jeffery PK. Chronic obstructive pulmonary disease: histopathology, inflammation and potential therapies. Pulm Pharmacol Ther. 2007;20(5):462-72. doi: 10.1016/j.pupt.2006.04.003. Epub 2006 May 6.
Barnes PJ. Inflammatory mechanisms in patients with chronic obstructive pulmonary disease. J Allergy Clin Immunol. 2016 Jul;138(1):16-27. doi: 10.1016/j.jaci.2016.05.011. Epub 2016 May 27.
Barnes PJ. Cellular and molecular mechanisms of chronic obstructive pulmonary disease. Clin Chest Med. 2014 Mar;35(1):71-86. doi: 10.1016/j.ccm.2013.10.004. Epub 2013 Dec 12.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
COPD and exercise
Identifier Type: -
Identifier Source: org_study_id