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.
UNKNOWN
NA
100 participants
INTERVENTIONAL
2016-06-01
2019-11-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effect of Hypoxic Conditioning on Cerebrovascular Health in the Elderly
NCT05048680
Evaluation of the Response to Hypoxia at Rest and During Exercise in a Healthy Subject After a Cryostimulation Exposure
NCT06174480
Effects of Different Moderate-intensity Exercise Methods on Health in the Elderly
NCT05207501
An Investigation Into the Effects of Acute Exercise on Activities of Daily Living and Cognition in Older Adults
NCT06085235
Stimulating Engagement in Daily and Physical Activities Among Older Adults Receiving Homecare Services (Part of Basic Care Revisited)
NCT02904889
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.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Brisk walking 1
1 time a week of 9 months brisk walking
Brisk walking
Prospective randomized clinical trial with 2 intervention groups and 1 control group.
Brisk walking 3
3 times a week of 9 months brisk walking
Brisk walking
Prospective randomized clinical trial with 2 intervention groups and 1 control group.
Control group
No brisk walking session
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Brisk walking
Prospective randomized clinical trial with 2 intervention groups and 1 control group.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Living in a nursing home of Mutualité Française de la Loire, France
* Being able to walk without human aid
* Being able to speak and write French
* Being inactive (less than 1 hours of physical activity per week)
* Having a normal sinus rhythm
* Being affiliated to the social welfare system
* Signing the informed consent form
Exclusion Criteria
* Suffering from cardiac or respiratory pathologies that contraindicate physical activity
* Serious comorbidities contraindicating physical activity
* Diagnosed cardiac pathologies that prevent heart rate variability analysis: congestive heart failure, cardiac pacemaker, implantable cardioverter defibrillator, serious ventricular rhythm troubles, atrial fibrillation, atrial flutter.
* Persons under legal protection
60 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University Hospital of Saint-Etienne
OTHER
University of Lyon
OTHER
Clinique Mutualiste Chirurgicale de la Loire
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
David HUPIN, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
University Hospital of Saint-Etienne
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
French Loire Mutuality
Saint-Etienne, , France
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2016-A00068-43
Identifier Type: REGISTRY
Identifier Source: secondary_id
2016-08
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.