CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 100 enrolled
Drug / intervention
Percutaneous neuromodulation. +1 moreother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06695949
NCT06695949N/ACompleted

Comparison of Percutaneous Neuromodulation and Therapeutic Exercise in Patients With Nonspecific Chronic Neck Pain: A Randomized Clinical Trial

Universidad de Almeria·interventional·Posted Nov 19, 2024·Updated Jan 21, 2026

In Brief

A clinical study evaluating Percutaneous neuromodulation. and Therapeutic Exercise. for Neck Pain and Chronic Pain. Completed, enrolled 100 participants across 1 site.

Detailed Summary

The aim of this study is to compare the effects of applying percutaneous neuromodulation with performing only therapeutic exercise in patients with non-specific chronic neck pain.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesSpain
Collaborators--

Timeline

N/ACompletedFinished
20252026
First PostedNov 19, 2024
Enrollment StartMay 28, 2025
Primary CompletionJul 31, 2025
Study CompletionSep 15, 2025
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 1.6 years ago

Interventions

Percutaneous neuromodulation.other

Percutaneous neuromodulation therapy involves inserting several fine needle electrodes 2 cm to 5 cm deep into the skin to target the muscle and surrounding soft tissues. A low-voltage electric current is then passed through these needles, which is hypothesized to improve muscle function by altering the pain signals traveling from the painful muscle to the brain, enhance blood flow to the painful area to promote healing, reduce inflammation and soreness, and increase muscle endurance, strength, and balance.

Therapeutic Exercise.other

These participants (n=50) will engage in resistance training for the cervical flexor muscles, following a progressive exercise program in a supine position with the head comfortably supported, as described by Falla et al. (2008). Participants will perform these exercises with a frequency of 3 days a week for 6 weeks, with each session lasting 30 minutes.