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Clinical Trials/NCT05596019
NCT05596019
Completed
Not Applicable

Effectiveness of Specific Neurodynamic Exercises Compared With Non-specific Exercises on Disability and Neck Pain in Women Older Than 65 Years

University of Salamanca1 site in 1 country56 target enrollmentJuly 16, 2022
ConditionsNeck Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Neck Pain
Sponsor
University of Salamanca
Enrollment
56
Locations
1
Primary Endpoint
Neck disability
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

This is a randomized, parallel, double-blind clinical trial. The main objective is to compare the efficacy of multimodal exercise with specific neurodynamic exercises and multimodal exercise with non-specific exercises in disability and neck pain in women older than 65 years.

The intervention in both groups will be carried out for 4 weeks, with three weekly sessions. Two evaluations will be carried out, a pre-intervention evaluation and a post-intervention evaluation. We will assess neck pain, disability, upper limb strength, cervical mobility, cervical pressure pain thresholds, kinesiophobia and catastrophism.

Registry
clinicaltrials.gov
Start Date
July 16, 2022
End Date
January 20, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Roberto Méndez Sánchez

Associate Professor

University of Salamanca

Eligibility Criteria

Inclusion Criteria

  • Women older than 65 years.
  • Neck pain

Exclusion Criteria

  • Pacemakers
  • Fibrillations
  • Cardiac pathology or uncontrolled hypertension
  • History of severe trauma/recent cervical surgery
  • Uncontrolled systemic and inflammatory pathologies
  • Congenital collagen compromise
  • Presence of difficulties in performing the Initial Evaluation tests
  • Language barriers
  • Pending litigation or legal claim

Outcomes

Primary Outcomes

Neck disability

Time Frame: four weeks

The Neck Disability Index (NDI) will be used. It is a modification of the Oswestry Low Back Pain Disability Index. It is a scale used to measure disability associated with cervical pain due to acute or chronic conditions. He has 10 items: 7 related to activities of daily living, 2 related to pain and 1 related to concentration. The test can be interpreted with a maximum score of 50.

Pain intensity

Time Frame: four weeks.

Numerical Pain Rating Scale (NPRS) will be used. It is a scale used to quantify the patient's pain level on an 11-point numerical scale 0-10 with 0 being "no pain" and 10 being the "worst possible pain."

Secondary Outcomes

  • Pressure pain threshold(four weeks)
  • Kinesiophobia(four weeks)
  • Cervical range of motion(four weeks)
  • Hand grip strength(four weeks)
  • upper limb strength(four weeks)
  • Catastrophism(four weeks)

Study Sites (1)

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