- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02301559
The Influence of the Method Pilates in Women With Primary Dysmenorrhea
November 25, 2014 updated by: Juliany Marques Abreu da Fonseca, Universidade Estadual do PiauÍ
The Influence of the Method Pilates in Life Quality, Intensity of Pain and Flexibility of Women With Primary Dysmenorrhea
Primary dysmenorrhea is the result of hypercontractility and uterine vascular ischemia is the most common gynecologic complaints in young women.
According to the intensity of symptoms may impair daily living, work and leisure activities.
Pilates brings the concept of moving the body for the recovery, maintenance and promotion of health through exercises that stimulate circulation, improving physical conditioning, flexibility and proper postural alignment, and promote improvement in the levels of body awareness, coordination and muscle control.
In this sense, the objective is to investigate the effects of pilates in the symptomatology of primary dysmenorrhea.
This is a study to be developed with students of Physical Therapy from the State University of Piauí-UESPI presenting with primary dysmenorrhea compatible clinical picture.
A questionnaire will be used for research.
The students with the framework of dysmenorrhea that meet the inclusion criteria will be assessed for anthropometric parameters, pain, flexibility, indirect assessment of contraction of transversus abdominis and quality of life before and after the treatment protocol using the pilates method, often 3 weekly meetings, totaling 20 sessions.
Study Overview
Detailed Description
The objective is to investigate the effects of pilates in the symptomatology of primary dysmenorrhea.
This is a study to be developed with students of Physical Therapy from the State University of Piauí-UESPI presenting with primary dysmenorrhea compatible clinical picture.
A questionnaire will be used for research.
The students with the framework of dysmenorrhea that meet the inclusion criteria will be assessed for anthropometric parameters, pain, flexibility, indirect assessment of contraction of transversus abdominis and quality of life before and after the treatment protocol using the pilates method, often 3 weekly meetings, totaling 20 sessions.
Study Type
Interventional
Enrollment (Anticipated)
11
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Piaui
-
Teresina, Piaui, Brazil, 64000000
- Recruiting
- Universidade Estadual do PiauÍ
-
Contact:
- Juliany M A da Fonseca, Principal
- Phone Number: (86)81644967
- Email: juliany.markes@hotmail.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 25 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Voluntary
- Female
- 18-25 years old
- Enrolled in Physiotherapy course at the State University of Piauí- UESPI, with symptoms compatible with primary, nulliparous dysmenorrhoea, who have regular menstrual cycle and who agree to participate spontaneously in the research, by signing a term of informed consent (Appendix a) in accordance with Resolution 466/2012.
- Participation in the survey did not veto the use of analgesic or contraceptive by the participants.
- All are oriented to maintaining the habits of life - food, work and leisure activities, medications - during the exercises
Exclusion Criteria:
- Will not be included in the selected research volunteers that do not show symptoms and characteristics consistent with primary dysmenorrhoea according to the questionnaire, and those who accept not participate and / or not signing the consent form sample.
- As criteria for inclusion are also not chronic back pain, regular physical activity (3 or more times per week), women with pathological picture associated or malformation of the pelvic organs (secondary dysmenorrhea), or those that make use of device Intra- uterus (IUD).
- Will be excluded from the sample participants who submit two consecutive absences to care.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Pilates Group
Pilates Group, Pilates exercises, 20 sessions, lasting 40 minutes each, 3 times per week.
Soil and ball exercises, with emphasis on the pelvic region.
The program began with the work of breathing and postural correction, with warm-up exercises or preparatory, followed by the framework of classical movements of the method.
|
Pilates exercises with emphasis on pelvic region
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain, Visual analog scale
Time Frame: two months
|
Effects of pilates method in pain
|
two months
|
|
Quality of health, score Short Form-36
Time Frame: two months
|
Effects of pilates method in quality of health
|
two months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Flexibility, finger-ground test
Time Frame: two months
|
Effects of pilates method in flexibility
|
two months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Juliany M A da Fonseca, Principal, Universidade Estadual do PiauÍ
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
September 1, 2014
Primary Completion (Actual)
November 1, 2014
Study Completion (Anticipated)
December 1, 2014
Study Registration Dates
First Submitted
November 16, 2014
First Submitted That Met QC Criteria
November 25, 2014
First Posted (Estimate)
November 26, 2014
Study Record Updates
Last Update Posted (Estimate)
November 26, 2014
Last Update Submitted That Met QC Criteria
November 25, 2014
Last Verified
November 1, 2014
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 04008402357J
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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