Pilates to Treat Neck Pain

NCT ID: NCT02433821

Last Updated: 2015-05-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

64 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-02-29

Study Completion Date

2014-05-31

Brief Summary

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The neck pain comes from disturbances related to the cervical spine, of multifactorial origin and is considered a frequent problem of disability.

Pilates is a physical conditioning method that has been widely used to improve posture and develop body awareness.

The aim of this study is to assess the impact of the Pilates method in the control of pain, function and quality of life in patients with chronic mechanical neck pain.

Methods: 64 patients with chronic mechanical neck pain will be selected and randomized into two groups: intervention and control. Both groups will be assessed for pain, function, quality of life and medication intake.

The intervention group will hold Pilates sessions for three months, with two sessions per week. The control group will continue with the usual drug treatment. Both groups will be instructed to use 750mg acetaminophen every 6 hours if there is pain, but consumption of the drug will be controlled.

Although the symptoms of neck pain are common in the population, no study has investigated the effects of the Pilates method as a possible treatment for neck pain. The hypothesis is that the Pilates method can offer benefits to these patients.

Detailed Description

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Conditions

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Mechanical Neck Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Pilates Group

The group will realize 2 classes per week, lasting one our, of Pilates under supervision of a trained instructor. The training program will last 3 months.

Group Type EXPERIMENTAL

Pilates

Intervention Type OTHER

Control group

The patients will keep the drug treatment and will be keep in a waiting list. After the 180 days of study the will be invited to realize the Pilates training.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Pilates

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* People with diagnosis of chronic mechanical neck pain and symptoms of pain in the lower region of spine, between the occipital and the first thoracic vertebra, for more than three months.
* Pain between 3 and 8 on the numerical pain scale
* Age between 18 and 65
* Both genders
* Agree to take part in the study and sign the terms of agreement

Exclusion Criteria

* Fibromyalgia
* Previous traumatic injuries in the spine
* Infections and inflammation in the spine cervical pain radiating to upper limbs
* The practice of physical activity started or altered in the last 3 months
* Visual deficiency not corrected by glasses, disturbance in the central nervous system, hearing deficiency making the use of the method impossible.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Federal University of São Paulo

OTHER

Sponsor Role lead

Responsible Party

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Luciana de Araujo Cazotti

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Jamil Natour, PhD

Role: STUDY_CHAIR

Federal University of São Paulo

Locations

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Universidade Federal de Sao Paulo

São Paulo, São Paulo, Brazil

Site Status

Countries

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Brazil

References

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de Araujo Cazotti L, Jones A, Roger-Silva D, Ribeiro LHC, Natour J. Effectiveness of the Pilates Method in the Treatment of Chronic Mechanical Neck Pain: A Randomized Controlled Trial. Arch Phys Med Rehabil. 2018 Sep;99(9):1740-1746. doi: 10.1016/j.apmr.2018.04.018. Epub 2018 May 9.

Reference Type DERIVED
PMID: 29752907 (View on PubMed)

Other Identifiers

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CEP_UNIFESP-0208/11

Identifier Type: -

Identifier Source: org_study_id

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