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
20 participants
INTERVENTIONAL
2018-01-03
2018-07-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
MATERIAL-METHODS: This study has been reviewed by Ethics Committee of Non-Interventional Researches of the University of Medipol in Istanbul and its ethical conformity has been approved. (10840098-604.01.01-E.45484). Participants were informed of the voluntary consent form and signed the consent form.
Participants 20 sedentary women were included in the study between 30-50 years of age.
Evaluations
Demographic information (Age, Occupation, Height, Weight) of the persons will be recorded.Functional Movement Analysis; Postural Analysis, Depression level; Health Related Life quality will be recorded.
Application Pilates exercises will be applied by a qualified physiotherapist with an internationally recognized certificate on the subject. Participants will be asked to come up with suitable outfits. the exercise room will be set at the ideal temperature and well ventilated. The exercises to be done in the form of group exercises will be started with an entry level, and the level of the exercises will be increased appropriately in the following weeks. Each group will consist of no more than 10 people and the exercises will continue for three sessions per week for 12 weeks. The evaluations will be repeated before exercise, at the end of 12 weeks of exercise and after 3 months from finish of the exercise period.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Effect of Reformer Pilates on Functional Capacity, Balance, and Quality of Life in Sedentary Women
NCT07257731
The Effect of Pilates on Biopsychosocial Characteristics in the Covid-19 Pandemic
NCT05496634
Does Reformer Pilates Exercise Improve Cognitive Functions in Sedentary Women?
NCT05932004
Clinical Pilates and Aerobic Exercise in Menopause
NCT05764031
Acute Effects of Reformer, Cadillac, and Chair Pilates Appa-ratuses on Cardiac Autonomic Modulation and Flexibility
NCT07308626
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.
NON_RANDOMIZED
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Functional Movement Screen
Pilates Group Exercises
For 12 weeks, 3 repetitions per week
Posture Analysis
Pilates Group Exercises
For 12 weeks, 3 repetitions per week
Depression Level
Pilates Group Exercises
For 12 weeks, 3 repetitions per week
Quality of Life
Pilates Group Exercises
For 12 weeks, 3 repetitions per week
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Pilates Group Exercises
For 12 weeks, 3 repetitions per week
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Not to have a systemic disease leading preventing from exercise.
* Not having had any exercise in the last 3 months.
Exclusion Criteria
* To feel pain, discomfort during tests.
30 Years
50 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Medipol University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Emre Serdar Vayvay
Lecturer
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Emre S Atalay, PhD
Role: PRINCIPAL_INVESTIGATOR
Saglik Bilimleri Universitesi
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Emre Serdar Atalay
Istanbul, , Turkey (Türkiye)
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.
Guler Atalay
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
10840098-604.01.01-E.45484
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.