NCT02301559

Brief Summary

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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
11

participants targeted

Target at below P25 for not_applicable pain

Timeline
Completed

Started Sep 2014

Shorter than P25 for not_applicable pain

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2014

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2014

Completed
15 days until next milestone

First Submitted

Initial submission to the registry

November 16, 2014

Completed
10 days until next milestone

First Posted

Study publicly available on registry

November 26, 2014

Completed
5 days until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2014

Completed
Last Updated

November 26, 2014

Status Verified

November 1, 2014

Enrollment Period

2 months

First QC Date

November 16, 2014

Last Update Submit

November 25, 2014

Conditions

Outcome Measures

Primary Outcomes (2)

  • Pain, Visual analog scale

    Effects of pilates method in pain

    two months

  • Quality of health, score Short Form-36

    Effects of pilates method in quality of health

    two months

Secondary Outcomes (1)

  • Flexibility, finger-ground test

    two months

Study Arms (1)

Pilates Group

EXPERIMENTAL

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.

Behavioral: Pilates exercises

Interventions

Pilates exercises with emphasis on pelvic region

Pilates Group

Eligibility Criteria

Age18 Years - 25 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Voluntary
  • Female
  • 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

You may not qualify if:

  • 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.
  • Will be excluded from the sample participants who submit two consecutive absences to care.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Universidade Estadual do Piaui

Teresina, Piauí, 64000000, Brazil

RECRUITING

MeSH Terms

Conditions

Pain

Interventions

Exercise Movement Techniques

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Physical Therapy ModalitiesTherapeutics

Study Officials

  • Juliany M A da Fonseca, Principal

    Universidade Estadual do PiauÍ

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Juliany M A da Fonseca, Principal

CONTACT

Juliany M A da Fonseca, Principal

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
academic physiotherapy

Study Record Dates

First Submitted

November 16, 2014

First Posted

November 26, 2014

Study Start

September 1, 2014

Primary Completion

November 1, 2014

Study Completion

December 1, 2014

Last Updated

November 26, 2014

Record last verified: 2014-11

Locations