NCT06759025

Brief Summary

In this study, the primary aim was to examine the relationship between kinesiophobia and clinical outcomes in individuals with chronic neck pain. The secondary aim was to compare the level of neck disability, pain, endurance, functionality, muscle and grip strength, and quality of life in individuals with chronic neck pain who had and did not have kinesiophobia; and to determine the determinants of kinesiophobia in patients with chronic neck pain.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
120

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jan 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 30, 2024

Completed
7 days until next milestone

First Posted

Study publicly available on registry

January 6, 2025

Completed
7 days until next milestone

Study Start

First participant enrolled

January 13, 2025

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 4, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 10, 2025

Completed
Last Updated

April 20, 2026

Status Verified

April 1, 2026

Enrollment Period

6 months

First QC Date

December 30, 2024

Last Update Submit

April 17, 2026

Conditions

Chronic Neck Pain

Keywords

chronic neck painkinesiophobiaquality of lifefunctionality

Outcome Measures

Primary Outcomes (1)

  • Tampa Kinesiophobia Scale

    24 weeks

Secondary Outcomes (4)

  • Visual Analog Scale

    24 weeks

  • Neck Disability Index

    24 weeks

  • Disabilities of the Arm, Shoulder, and Hand Questionnaire

    24 weeks

  • SF-12 Quality of Life Scale

    24 weeks

Study Arms (1)

Study Group

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients who meet the inclusion criteria and are receiving treatment at the Kırşehir Education and Research Hospital Physical Therapy and Rehabilitation Center will constitute the population.

You may qualify if:

  • Neck pain complaints that have been ongoing for at least 3 months
  • Between the ages of 18-65
  • Complaints of numbness and tingling
  • Volunteer who can cooperate during communication

You may not qualify if:

  • History of spinal trauma or surgery
  • Neurological, rheumatological, systemic or musculoskeletal problems that affect movement
  • Serious comorbidities (such as advanced renal failure, previous history of CVA, malignancy)
  • Muscle weakness

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kirsehir Ahi Evran University

Kırşehir, Merkez, 40100, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Kinesiophobia

Condition Hierarchy (Ancestors)

Phobic DisordersAnxiety DisordersMental Disorders

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr. Lecturer

Study Record Dates

First Submitted

December 30, 2024

First Posted

January 6, 2025

Study Start

January 13, 2025

Primary Completion

July 4, 2025

Study Completion

October 10, 2025

Last Updated

April 20, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Locations

TU(1)