GPR vs Manual PT for Chronic Neck Pain
- Conditions
- Nonspecific Chronic Neck Pain
- Interventions
- Other: Global Postural Re-educationOther: Standard manual physical therapy
- Registration Number
- NCT01947231
- Lead Sponsor
- University of Bologna
- Brief Summary
Effective treatment for nonspecific chronic neck pain is a clinical challenge. Patients will be randomized into two groups to compare the outcomes of Global Postural Re-education (GPR) with standard manual physical therapy on with respect to pain, function, kinesiophobia, range of motion, perceived effect, and satisfaction.
- Detailed Description
These study will use two groups: one to receive GPR which is a systematic method of addressing musculoskeletal pain and related functional deficits and the other to receive "usual care" manual PT which will be individualized to the patient's condition. Usual care will include techniques commonly used in clinical practice selected by the physical therapist after initial examination. After nine weeks of treatment, baseline measures will be re-evaluated. After conclusion of the first phase of the study, patients who were randomized to the "usual care" group will cross-over and receive GPR.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 100
-nonspecific neck pain lasting at least 3 months
- acute or subacute cervical pain
- specific or known cause of pain
- central or peripheral neurological signs
- systemic pathology
- rheumatologic pathology
- neuromuscular pathology
- cognitive impairment
- surgical intervention in the last 6 months prior to study
- physical therapy treatment in the last 6 months prior to study
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Global Postural Re-education Global Postural Re-education Global Postural Re-education is delivered in a single treatment session each week for nine weeks. Standard manual physical therapy Standard manual physical therapy Standard manual physical therapy is delivered in a single treatment session each week for 9 weeks.
- Primary Outcome Measures
Name Time Method Pain 9 weeks after start of intervention The investigators assessed this outcome with a Visual Analogue Scale (VAS).
Cervical Functional Limitations 9 weeks after start of intervention The investigators assessed this outcome with the Neck Disability Index.
- Secondary Outcome Measures
Name Time Method Cervical Range of Motion 9 weeks after start of intervention The investigators assessed this outcome with the CROM-Deluxe which is an inclinometer that is placed on the subject's head to measure cervical range of motion.
Patient Satisfaction 9 weeks after start of intervention The investigators assessed this outcome with the Physical Therapy Patient Satisfaction Questionnaire - Italian Version which has established psychometric properties.
Kinesiophobia 9 weeks after start of intervention The investigators assessed this outcome with the Tampa Scale of Kinesiophobia.
Self-reported Global Effect of the Intervention 9 weeks after start of intervention The investigators assessed this outcome with a Global Perceived Effect scale which measures the subject's self-reported improvement or deterioration following the intervention.
Trial Locations
- Locations (1)
Policlinico S. Orsola-Malpighi
🇮🇹Bologna, Emiglia-Romagna, Italy