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Clinical Trials/NCT03218644
NCT03218644CompletedNot Applicable

Effectiveness of a Propioceptive Exercise Program in Subjects With Inespecific Neck Pain

University of Valencia1 site in 1 country47 target enrollmentStarted: July 14, 2017Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
47
Locations
1
Primary Endpoint
Intensity of Pain

Study Overview

Brief Summary

Introduction: Neck pain is among the most common and costly for industrialized societies. It is difficult to know the exact structure causing the pain so most are considered as non-specific neck pain. There is a correlation between the alteration of craneocervical proprioception and neck pain. The evidence for treatment with proprioceptive exercises is very limited.

Objective: To know the efficacy of a proprioceptive exercise program for neck pain and to compare its effects with a cervical mobility program.

Materials and Methods: Subjects between 18-65 years old with non-traumatic neck pain are included. They will be randomized into two groups of exercises: proprioception or mobility, which will be developed over a period of two weeks, every day, with a total of 10 sessions per patient.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Neck pain (NAD I-II) of recent onset (0-3 months)

Exclusion Criteria

  • •Cognitive difficulties
  • •Lack of commitment to attend sessions
  • •Subjects with pacemakers or defibrillators
  • •Being receiving another physiotherapeutic treatment
  • •Other pathologies

Arms & Interventions

Control group

Active Comparator

Follow the usual treatment and perform the exercises of cervical mobility before a mirror.

Intervention: Mobility exercises (Other)

Experimental group

Experimental

The same procedure is followed by substituting proprioceptive exercises for craniocervical sensorimotor control with a laser instrument located on the patient's head and a target.

Intervention: Proprioception exercises (Other)

Outcomes

Primary Outcomes

Intensity of Pain

Time Frame: four weeks

Visual Analogue Scale (VAS) was used to register the pain. The VAS is a 10-point rating scale.

Secondary Outcomes

  • Pain points(four weeks)
  • Head Repositioning Test(four weeks)
  • Cervical movement range (CROM)(four weeks)
  • Neck Disability(four weeks)
  • Health status(four weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

GEMMA V ESPÍ LÓPEZ, PhD

Principal Investigator

University of Valencia

Study Sites (1)

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