RECRUITING

How Dry Needling At the Neck Affects Shoulder Movement, Strength, Pain, and Shoulder Circulation

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Segmental facilitation, originally proposed by Korr in the 1950s, suggests that certain spinal segments can become hyperexcitable, leading to chronic pain development. In a facilitated segment, neurons governing sensory, motor, and autonomic functions are in a state of heightened sensitivity, making them responsive to normally weak stimuli. Clinical signs include non-fatigable muscle weakness, brisk reflexes, muscle hypertonicity, tenderness upon palpation, and trophic changes like an orange-peel appearance in the affected segment's innervated areas. It's hypothesized that increased synaptic excitability in facilitated segments could cause vasoconstriction and reduced blood flow, contributing to trophic changes and muscle hypertonicity. Manual therapies like dry needling have been shown to alleviate muscle inhibition in the extremities. Previous studies have demonstrated that mobilization of the C5-6 joint can reduce non-fatigable weakness in shoulder external rotators primarily innervated by these segments. However, the neurophysiological effects of dry needling (DN) on muscle inhibition due to a facilitated segment remain unclear. While DN has been observed to increase local tissue blood flow, its potential to mitigate the clinical signs of segmental facilitation is uncertain. While DN has been observed to increase local tissue blood flow, its potential to mitigate the clinical signs of segmental facilitation is uncertain. Therefore, this project aims to investigate whether DN applied at a facilitated segment could normalize blood flow to its associated muscles. Specifically, this study will explore whether DN at the C5-6 level improves blood flow in the infraspinatus muscle, enhances shoulder range of motion, and influences muscle strength over time. The secondary purpose is to determine whether C5-6 DN will reduce the number of tender points in the muscles supplied by C5-6.

Official Title

Effects of Dry Needling of C5-C6 on Shoulder Range of Motion, Strength, Tender Points, and Blood Flow

Quick Facts

Study Start:2024-12-01
Study Completion:2025-11-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06705634

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 65 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * adults 18-65 years of age
  2. * non-specific neck-shoulder pain (over the upper trapezius or the infraspinatus area) with an average pain ≥ 2/10 on the Numeric Pain Rating Scale (score range from 0-10, 0 = no pain, 10 = unbearable pain)
  3. * at least one tender point in one of the 5 muscles: cervical paraspinal near C5-C6 spinal segment, rhomboids, supraspinatus, infraspinatus, and deltoid.
  1. * Active systemic arthritis (e.g., rheumatoid arthritis, psoriatic arthritis)
  2. * Traumatic brain injury
  3. * Stroke Seizures/epilepsy
  4. * Neurological disease (e.g., multiple sclerosis, muscular dystrophy, Parkinson's, spinal cord compression)
  5. * Acute or History of Fracture of cervical spine
  6. * Acute or History of Fracture of the shoulder
  7. * Circulation/vascular problems (e.g., Raynaud's)
  8. * Cancer
  9. * Uncontrolled diabetes/high blood sugar
  10. * Currently pregnant
  11. * Previous neck surgery
  12. * Previous arthroscopic shoulder surgery in the last 5 years
  13. * Previous shoulder arthoplasty
  14. * Taking an anticoagulant (blood thinner)
  15. * Allergic to ultrasound gel

Contacts and Locations

Study Contact

Jace Brown, DPT, PhD
CONTACT
2146897716
jbrown34@twu.edu
Sharon Wang-Price, PhD
CONTACT
214-689-7715
swang@twu.edu

Study Locations (Sites)

Texas Woman's University T. Boone Pickens Institute of Health Sciences
Dallas, Texas, 75235
United States

Collaborators and Investigators

Sponsor: Texas Woman's University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-12-01
Study Completion Date2025-11-01

Study Record Updates

Study Start Date2024-12-01
Study Completion Date2025-11-01

Terms related to this study

Keywords Provided by Researchers

  • neck pain
  • shoulder pain
  • muscle pain
  • dry needling
  • neck tightness
  • shoulder tightness

Additional Relevant MeSH Terms

  • Dry Needling Technique
  • Neck Pain Musculoskeletal
  • Shoulder Pain
  • Neck Pain
  • Dry Needling