Pilates to Treat Neck Pain

Federal University of São Paulo

Status and phase: Completed; Phase 3

Conditions: Mechanical Neck Pain

Treatments: Other: Pilates

Study type: Interventional

Funder types: Other

Identifiers

NCT02433821

CEP_UNIFESP-0208/11

Details and patient eligibility

About

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.

Enrollment: 64 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

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.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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64 participants in 2 patient groups

Pilates Group

Experimental group

Description:

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.

Treatment:

Other: Pilates

Control group

No Intervention group

Description:

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.