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A Novel Device for Neck Pain in Active-duty Military Personnel With Forward Head Posture.

Primary Purpose

Neck Pain

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Cervigard Neck Collar
Sponsored by
Kessler Foundation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Neck Pain

Eligibility Criteria

18 Years - 45 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • DEERS Eligible
  • Age 18 and 45 year old (inclusive)
  • Neck pain duration ≥ 3 months without neurological signs and have been seen by a provider.
  • Conventional treatments have not decreased neck pain
  • Neck pain ≥ 4 on a 0-10 point numerical rating scale (0 = "no pain", 10 = "maximum pain")
  • Forward head posture, indicated by forward placement of the head relative to the shoulders.

Exclusion Criteria:

  • History of a tumor in the cervical spine and/or head/neck region within the past 6 months.
  • Infection involving the cervical spine and/or head/neck region within the past 6 months.
  • Generalized medical disorders that would weaken the vertebrae or other tissue structures within the cervical spine region.
  • Fracture that is acute and/or still healing
  • Spinal deformities (e.g. Fixed kyphosis, Ankylosing spondylosis)
  • Medical and/or psychological condition that would preclude safe participation

Sites / Locations

  • Walter Reed National Military Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention

Waitlist Control

Arm Description

Cervigard Neck Collar, which is a device used to treat neck pain caused by forward head posture.

This group will receive no intervention for 6 weeks after enrollment. They will receive the device after 6 weeks.

Outcomes

Primary Outcome Measures

Change in Numerical Pain Rating Scale score
Neck pain intensity will be assessed using the Numerical Rating Scale. Subjects will be asked to rate their average pain during the past week using an 11-point scale (i.e. 0-10) anchored at the ends by "no pain" and "worst pain ever experienced."

Secondary Outcome Measures

Change in Neck Disability Index scores
The Neck Disability Index is a disease-specific measure of neck pain-related sequelae. It includes 10 sections designed to capture different aspects of everyday life and how neck pain potentially affects those areas. Examples include personal care, lifting, headaches, concentration, work, and sleep.
Change in lordotic angle of the cervical spine
The angle of the curve of the cervical spine will be measured using a custom computer program in blinded and random fashion.
Change in head position
The position of the cranium relative to the 7th cervical vertebra will be measured using a custom computer program in blinded and random fashion.

Full Information

First Posted
June 23, 2022
Last Updated
October 4, 2023
Sponsor
Kessler Foundation
Collaborators
The Geneva Foundation, Walter Reed National Military Medical Center, Uniformed Services University of the Health Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT05433025
Brief Title
A Novel Device for Neck Pain in Active-duty Military Personnel With Forward Head Posture.
Official Title
Safety and Treatment Effect of a Novel Device for Neck Pain in Active-duty Military Personnel With Forward Head Posture.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 20, 2022 (Actual)
Primary Completion Date
June 30, 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kessler Foundation
Collaborators
The Geneva Foundation, Walter Reed National Military Medical Center, Uniformed Services University of the Health Sciences

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes

5. Study Description

Brief Summary
Neck pain is a common complaint among active duty military personnel, and can have tremendous impacts on quality of life and participation in duty-related activities. Treatments for spinal pain in military personnel are typically multimodal, relying upon physical therapy, pharmacological agents, spinal manipulation, and psychotherapy. However, there does not exist a wide body of evidence to support many of these treatments in active-duty military. The Cervigard neck collar was designed to treat posture-related neck pain with minimal effort and time required for treatment by the patient. However, this has yet to be tested experimentally. The objective of this study is to evaluate the treatment effect and safety of a novel device for the treatment of neck pain using self-reported pain and function measures, as well as objective radiological measures of cervical lordosis and head posture. Participants will be randomized to be fitted with and receive the Cervigard neck collar either immediately, or 6-weeks after being screened. Participants will complete neck pain and function questionnaires, and have cervical X-Rays collected at screening, treatment, 6 weeks, and 12 weeks (for the immediate group). Participants will be instructed to wear the collar every day for the duration of the trial. Self-reported neck pain and function measures will be collected, as well as cervical X-Rays, protocol adherence measures, and adverse events. The intervention is expected to reduce neck pain/discomfort, improve function, and improve cervical lordosis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neck Pain

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
Cervigard Neck Collar, which is a device used to treat neck pain caused by forward head posture.
Arm Title
Waitlist Control
Arm Type
No Intervention
Arm Description
This group will receive no intervention for 6 weeks after enrollment. They will receive the device after 6 weeks.
Intervention Type
Device
Intervention Name(s)
Cervigard Neck Collar
Intervention Description
A device used to treat neck pain caused by forward head posture
Primary Outcome Measure Information:
Title
Change in Numerical Pain Rating Scale score
Description
Neck pain intensity will be assessed using the Numerical Rating Scale. Subjects will be asked to rate their average pain during the past week using an 11-point scale (i.e. 0-10) anchored at the ends by "no pain" and "worst pain ever experienced."
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Change in Neck Disability Index scores
Description
The Neck Disability Index is a disease-specific measure of neck pain-related sequelae. It includes 10 sections designed to capture different aspects of everyday life and how neck pain potentially affects those areas. Examples include personal care, lifting, headaches, concentration, work, and sleep.
Time Frame
6 weeks
Title
Change in lordotic angle of the cervical spine
Description
The angle of the curve of the cervical spine will be measured using a custom computer program in blinded and random fashion.
Time Frame
6 weeks
Title
Change in head position
Description
The position of the cranium relative to the 7th cervical vertebra will be measured using a custom computer program in blinded and random fashion.
Time Frame
6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: DEERS Eligible Age 18 and 45 year old (inclusive) Neck pain duration ≥ 3 months without neurological signs and have been seen by a provider. Conventional treatments have not decreased neck pain Neck pain ≥ 4 on a 0-10 point numerical rating scale (0 = "no pain", 10 = "maximum pain") Forward head posture, indicated by forward placement of the head relative to the shoulders. Exclusion Criteria: History of a tumor in the cervical spine and/or head/neck region within the past 6 months. Infection involving the cervical spine and/or head/neck region within the past 6 months. Generalized medical disorders that would weaken the vertebrae or other tissue structures within the cervical spine region. Fracture that is acute and/or still healing Spinal deformities (e.g. Fixed kyphosis, Ankylosing spondylosis) Medical and/or psychological condition that would preclude safe participation
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nathan Hogaboom, PhD
Phone
9733243584
Email
nhogaboom@kesslerfoundation.org
Facility Information:
Facility Name
Walter Reed National Military Medical Center
City
Bethesda
State/Province
Maryland
ZIP/Postal Code
20889
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marin Smith
First Name & Middle Initial & Last Name & Degree
Jenny Yuan, MD
First Name & Middle Initial & Last Name & Degree
Michelle Nordstrom, OTR/L
First Name & Middle Initial & Last Name & Degree
Matthew St. Laurent, OT

12. IPD Sharing Statement

Plan to Share IPD
No

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A Novel Device for Neck Pain in Active-duty Military Personnel With Forward Head Posture.

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