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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02046876
Other study ID # UMA-1301
Secondary ID
Status Completed
Phase N/A
First received December 24, 2013
Last updated January 24, 2014
Start date January 2013
Est. completion date June 2013

Study information

Verified date January 2014
Source University of Malaga
Contact n/a
Is FDA regulated No
Health authority Spain: Ethics Committee
Study type Interventional

Clinical Trial Summary

Chronic neck pain (CNP) is defined as pain or intense discomfort in the lateral or back of the neck with an establishment and/or persistence period of over 12 weeks.

The socio-economic system is seriously affected by chronic neck pain due to direct and indirect costs on the health system Physical exercise is used to improve physical function and reduce the symptoms of pain and stiffness due to chronic neck pain.

It has been demonstrated that therapeutic exercise in water is effective to improve functional capacity and symptoms in patients with chronic neck pain. In adition, health education and posture is an important component of the overall treatment of neck pain.

Interventions that integrate physical activity, adapted swimming and health education as an intervention for chronic neck pain sufferers have not been found. Furthermore the aim of this study is to analyse the effect of a physiothperapy treatment that combine adapted swimming, therapeutic exercise and health education in patients with chronic neck pain.

Hypothesis: the present intervention will be an effective tool to treat patients suffering chronic neck pain.

Methods: chronic neck pain patients from a community-based centre will be recruite participate in this prospective study.

Intervention: 60 min session: 30 min of land exercise dedicated to improve mobility, motor control, resistance and strengthening of the neck muscles, 30 min of adapted swimming with aerobic exercise keeping neutral neck position by using a snorkel. Health education will be provided by the physiotherapist before and during the sessions using a decalogue on chronic neck pain and constant repetition of brief advice.

Study outcomes: disability (Neck Disability Index), physical and mental health state and quality of life of patients (SF-12 and EuroQoL 5D respectively).

Differences between baseline data and that at the 8-week follow-up were calculated for all outcome variables.

Statistical Analysis: descriptive statistics. Analysis of the normal distribution of the variables using the KS-test. Comparison of variables pre - post intervencición: T-Student for parametric variables and Wilcoxon test for non parametric variables.

Data will be analysed descriptively and for statistical significance using Statistical Package for the Social Sciences (SPSS) (version 17.0 for Windows, Illinois, USA).


Recruitment information / eligibility

Status Completed
Enrollment 175
Est. completion date June 2013
Est. primary completion date June 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Suffers Neck Pain for more than 12 weeks.

- Delivery of informed consent.

Exclusion Criteria:

- Neck pain due to an identifiable cause.

- Surgery on the spine in the 12 month

- Traffic accident in the last 3 months

- Cervical radiculopathy

- Pregnancy.

- Patients who suffered a condition that could alter the effects of treatment

- People who could not swim and/or present treatment difficulty.

Study Design

Intervention Model: Single Group Assignment, Masking: Double Blind (Caregiver, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Multimodal Physiotherapy Program
Multimodal Physiotherapy Program integrates: physical land-based therapeutic exercise, adapted swimming and health education

Locations

Country Name City State
Spain Patronato Municipal de Deportes de Torremolinos Torremolinos Málaga

Sponsors (1)

Lead Sponsor Collaborator
University of Malaga

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Neck Disability Index Disability due to Chonic Neck Pain Change from baseline in NDI at 8 weeks (post-treatment) Yes
Primary Neck Disability Index Disability due to Chonic Neck Pain Change from baseline in NDI at 6 month (follow-up) Yes
Primary Neck Disability Index Disability due to Chonic Neck Pain Change from baseline in NDI at 12 month (follow-up) Yes
Secondary Short Form 12 General Health State Questionnaire pre and post intervention and 6 and 12 months of follow up Yes
Secondary EuroQoL 5 Dimensions Health Related Quality of Life Questionnaire pre and post intervention and 6 and 12 months of follow up Yes
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