Effects of Therapeutic Intervention Through Selective Functional Movement Assessment on Pain, Function, Balance and Gait in Patients With Chronic Nonspecific Neck Pain

May 21, 2023 updated by: Hyun-Joong Kim, Sahmyook University
According to the order of the physical examination, the scope of the problem is narrowed down by excluding the parts of the body that do not have problems and adjusting the load related to stability. A list of problems can be created through an algorithmic approach that guesses which structures will have problems through active or passive movement. This provides an optional therapeutic intervention.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Anticipated)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

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.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Adults between the ages of 18 and 65 who have experienced chronic neck pain for more than 12 weeks (Blanpied et al., 2017).
  • Those with more than moderate pain (4/10 cm) on the visual analogue scale (VAS) (Paksaichol et al., 2012).
  • Those with a neck disability index (NDI) of mild disability (5/50 score) or higher (Lluch et al., 2014).
  • Those who consented to participate in this study.

Exclusion Criteria:

  • Patients with severe pathology such as radiation pain due to intervertebral disc herniation or neurological signs consistent with tumor, whiplash injury, cervical vertebra fracture, or nerve root compression.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Personalized exercise
Behavioral: Personalized exercise
After selective functional movement evaluation, customized interventions for each patient
Active Comparator: Stabilization exercise
Behavioral: Stabilization exercise
Neck stabilization exercise and sensorimotor program
Active Comparator: General exercise
Behavioral: General exercise
General mobility exercise and strength exercise program

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
neck disability index
Time Frame: change from baseline neck disability index at 8weeks
The questionnaire was composed of 10 questions to provide information on how neck pain affects daily life.
change from baseline neck disability index at 8weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sahmyook University

Investigators

  • Principal Investigator: Dajeong Kim, MSc, Yongin 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 Major Dates

Study Start (Actual)

April 30, 2023

Primary Completion (Anticipated)

August 1, 2023

Study Completion (Anticipated)

August 10, 2023

Study Registration Dates

First Submitted

April 24, 2023

First Submitted That Met QC Criteria

May 21, 2023

First Posted (Actual)

May 23, 2023

Study Record Updates

Last Update Posted (Actual)

May 23, 2023

Last Update Submitted That Met QC Criteria

May 21, 2023

Last Verified

May 1, 2023

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 21040966ABN012212HSR2822

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Only information provided in the paper publication is included.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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