Pilates to Treat Neck Pain

Phase 3

Completed

• Conditions: Mechanical Neck Pain
• Interventions: Other: Pilates

• Registration Number: NCT02433821
• Lead Sponsor: Federal University of São Paulo

Brief Summary

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

Not available

Study Timeline

• Study Start: 2012-02
• Primary Completion: 2012-08
• Study First Submitted: 2013-04-08
• Study Completion: 2014-05
• Status Verified: 2015-04
• Study First Submitted QC: 2015-04-29
• Last Update Submitted: 2015-04-29
• Study First Posted: 2015-05-05
• Last Update Posted: 2015-05-05

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 64

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.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Pilates Group	Pilates	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.

Primary Outcome Measures

Name	Time	Method
Change in pain	Baseline, after 45, 90 and 180 days	Evaluated by visual analogue scale (VAS) from 0 to 10

Secondary Outcome Measures

Name	Time	Method
Change in function	Baseline, after 45, 90 and 180 days	Evaluated by the Neck Disability Index (score ranges from 0 to 50)
Change in Quality of life	Baseline, after 45, 90 and 180 days	Evaluated by the short form 36 (SF-36) questionnaire
Change in medication intake	After 45, 90 and 180 days from baseline	Patients fill out a specific form regarding the medication intake

Trial Locations

Locations (1)

Universidade Federal de Sao Paulo; 🇧🇷 Sao Paulo, SP, Brazil