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NCT02124304 · ClinicalTrials.gov registry record · NA

Cervical Activation During Elastic and Manual Resistance

A NA study, sponsored by Sport and Spine Rehab Clinical Research Foundation.

Completed
Registry status
NA
Development phase
30
Enrollment target

NCT02124304: Completed NA study, sponsored by Sport and Spine Rehab Clinical Research Foundation.

NCT02124304 is a NA study that has completed, run by Sport and Spine Rehab Clinical Research Foundation. The registered enrollment target is 30 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02124304, a NA study, has completed, sponsored by Sport and Spine Rehab Clinical Research Foundation.

COMPLETED
Registry status
NA
Development phase
30 participants
Enrollment target

Study Summary

Cervical pain is a condition that affects 14.6% of all adults annually. Of this annual prevalence, 37.3% experience persistent neck pain with periodic recurring episodes. The purpose of this study is to compare muscle activation patterns of the cervical musculature during exercises with elastic versus manual resistance in a neck pain and asymptomatic populations. Methods: A convenience sample of 15 healthy, physically active participants and 15 current patients diagnosed with non-radicular cervical pain will be recruited. Exclusionary criteria will include: current cervical or upper extremity injury (healthy group), history of neck surgery, corticosteroid treatment within the last two weeks, and radicular signs or symptoms. Surface electromyography will be used to quantify the activity level of the bilateral SCM, AS, Cervical Paraspinal (CP), and the Upper Trapezius (UT) muscles while performing a series of 6 exercises with elastic resistance using Thera-Band® Resistance Bands and manual resistance. The area will be prepped and surface electrodes placed on the corresponding muscles. The movement will be standardized by using the peak activation (PA) of each muscle during full flexion-extension movement to create a percentage of peak activation (%PA). The testing battery will consist of 6 exercises with elastic resistance and manual resistance, totaling 12 different trials. Each trial will involve 5 repetitions, each held for 5 seconds. The exercises will include cervical: extension, flexion, left rotation, right rotation, left side bending, and right side bending. The men will use the green and women will use the red Thera-Band® Resistance Band. The order of exercises will be randomized in to two parts to minimize the effect of fatigue. First, cervical flexion and extension with manual and elastic resistance will be randomized. Secondly, the remaining 8 exercises will be randomized. Following each exercise, the patient will rate their perceived level of exertion on

Primary Outcome

8 muscles during 12 exercises were analyzed in 30 subjects, totaling 2880 data points. At the beginning of the study, peak activation (PA) was assessed for each muscle during full flexion-extension, used as a reference exercise. For each subject, the EMG signals of the muscles during the 12 exercises were smoothed, rectified and analyzed using a root-mean-square algorithm and the greatest activation of each muscle was used. After the PA for each muscle was determined, it was compared to the PA o

Interventions

  • DEVICE Neck exercises using both manual and Thera-Band elasatic resistance

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2014-04
Est. Completion 2014-08
Phase NA

What the finished NCT02124304 record still lists

NCT02124304 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 1 intervention - of which Neck exercises using both manual and Thera-Band elasatic resistance is the first listed.

NCT02124304 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02124304 about?

NCT02124304 is a clinical study titled "Cervical Activation During Elastic and Manual Resistance". Cervical pain is a condition that affects 14.6% of all adults annually. Of this annual prevalence, 37.3% experience persistent neck pain with periodic recurring episodes. The purpose of this study is to compare muscle activation patterns of the cervical musculature during exercises with elastic vers...

What is the current status of trial NCT02124304?

This trial is currently completed. It is a NA study. The enrollment target is 30 participants. The study started on 2014-04. Estimated completion is 2014-08.

What interventions are being tested in trial NCT02124304?

The interventions under investigation include: Neck exercises using both manual and Thera-Band elasatic resistance (DEVICE).

Who is sponsoring clinical trial NCT02124304?

This trial is sponsored by Sport and Spine Rehab Clinical Research Foundation, which has 16 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02124304's enrollment target sits among peer trials

30 1593rd of 2000 higher than 299 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02124304, the US trial registry maintained by the National Library of Medicine. NCT02124304 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.