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RecruitingNCT05871775Updated May 23, 2023

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

An interventional study of Personalized exercise and Stabilization exercise in Chronic Nonspecific Neck Pain, sponsored by Sahmyook University. Recruiting at 1 site in Korea, Republic of. Per ClinicalTrials.gov, last updated 2023-05-23.

Sponsored by Sahmyook University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Aug 2023, 3 years 2 months ago, but the record still lists the study as recruiting.
  • Started Apr 2023; still recruiting 3 years 5 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Sex
All
01

Study summary

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.

02

Conditions studied

  • Chronic Nonspecific Neck Pain

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Keywords

  • exercise
  • neck pain
  • chronic pain
03

In context

Neck Pain

1,232 studies on the registry are indexed under Neck Pain; 255 are open to participants now.

This study's planned enrollment of 30 is below the median of 52 across 1,004 interventional studies indexed under Neck Pain.

Browse Neck Pain studies →

Lead sponsor

Sahmyook University is the lead sponsor of 42 studies on the registry; 11 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

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

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.
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    Personalized exercise

    Behavioral: Personalized exercise

  • Active comparator
    Stabilization exercise

    Behavioral: Stabilization exercise

  • Active comparator
    General exercise

    Behavioral: General exercise

Interventions

  • BehavioralPersonalized exercise

    After selective functional movement evaluation, customized interventions for each patient

  • BehavioralStabilization exercise

    Neck stabilization exercise and sensorimotor program

  • BehavioralGeneral exercise

    General mobility exercise and strength exercise program

06

What researchers measure

Primary outcomes

  1. neck disability index

    The questionnaire was composed of 10 questions to provide information on how neck pain affects daily life.

    Time frame: change from baseline neck disability index at 8weeks

07

Study locations

1 of 1 sites recruiting
  • Yongin University
    Yongin, 17092, Korea, Republic of
    Recruiting
08

References and documents

Individual participant data

Plan to share: No — Only information provided in the paper publication is included.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 23, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05871775
Lead sponsor
Sahmyook University
Responsible party
Hyun-Joong Kim (investigator, Sahmyook University) — Principal investigator
First posted
May 23, 2023
Start date
Apr 30, 2023
Primary completion
Aug 1, 2023 (estimated)
Completion
Aug 10, 2023 (estimated)
Last update
May 23, 2023

Study contacts

Dajeong Kim, MSc
Contact
kdj201305@naver.com
+82-10-5893-5498
Dajeong Kim, MSc
principal investigator · Yongin University

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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