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
60 participants
INTERVENTIONAL
2016-02-01
2018-03-25
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.
A Functional Exercise Program Improves Pain and Health Related Quality of Life in Patients With Fibromyalgia
NCT03682588
Effectiveness of Physical Exercise in Women With Fibromyalgia
NCT00498264
Strength Training in Fibromyalgia on Balance, Neuromuscular Performance and Symptoms
NCT05646641
Stretching and Strengthening Exercise in Fibromyalgia Patients
NCT01029041
Preference of Women With Fibromyalgia Undergoing a Three Different Volumes of Resistance Training
NCT06424743
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
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Intervention Group
Progressive resistance training program
Progressive resistance training program were performed twice a week for 12 weeks. The charge intensity was progressively increased from 40% to 80% of 1 repetition maximum. The following muscle groups were worked: trunk flexors and extensors, elbow flexors and extensors, knee flexors and extensors, hip abductors and adductors and shoulder abductors. In addition to strength training.
Educational Program
Structured education program were performed during one hour class once a week for five weeks
Control Group
Educational Program
Structured education program were performed during one hour class once a week for five weeks
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Progressive resistance training program
Progressive resistance training program were performed twice a week for 12 weeks. The charge intensity was progressively increased from 40% to 80% of 1 repetition maximum. The following muscle groups were worked: trunk flexors and extensors, elbow flexors and extensors, knee flexors and extensors, hip abductors and adductors and shoulder abductors. In addition to strength training.
Educational Program
Structured education program were performed during one hour class once a week for five weeks
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Feminine gender;
* Age between 18 and 65 years;
* Pain between 3 and 8 cm in the Numerical Pain Scale (END);
* Have not changed treatment for fibromyalgia in the past three months;
* Agree to participate in the study and sign the informed consent form.
Exclusion Criteria
* Other diseases that make it impossible to perform the exercises;
* Physical activity started or changed in the last three months;
* Physical therapy in the last six months;
* In litigation.
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Federal University of São Paulo
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Anamaria Jones
Professor
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
CEP UNIFESP 482056
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.