NCT07617623

Brief Summary

Chronic non-specific neck pain is a common musculoskeletal condition affecting a large proportion of the population worldwide. It is characterized by persistent neck pain lasting more than three months without a specific underlying pathology. Many patients experience ongoing symptoms such as pain, reduced range of motion, functional limitations, and psychological factors like kinesiophobia, which can negatively affect recovery and quality of life. Conventional physiotherapy, including supervised clinic-based rehabilitation, is widely used for the management of chronic non-specific neck pain. These programs typically involve exercise therapy and patient education; however, access to regular in-clinic treatment can be limited due to factors such as travel, cost, and time constraints. Telerehabilitation has emerged as an alternative approach that allows delivery of physiotherapy services through online platforms, improving accessibility and convenience for patients. In addition, pain neuroscience education (PNE) is an evidence-based strategy that helps patients understand pain mechanisms, reduce fear-avoidance behaviors, and improve treatment outcomes when combined with exercise therapy. Although both telerehabilitation and supervised clinic-based rehabilitation are effective, there is limited evidence directly comparing these two approaches when combined with standardized pain neuroscience education. Therefore, this randomized controlled trial aims to compare the effects of telerehabilitation with pain neuroscience education and supervised clinic-based rehabilitation with pain neuroscience education on pain intensity, functional disability, and kinesiophobia in individuals with chronic non-specific neck pain.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
45

participants targeted

Target at P25-P50 for not_applicable

Timeline
4mo left

Started Jun 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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

Study Progress36%
Jun 2026Nov 2026

First Submitted

Initial submission to the registry

May 23, 2026

Completed
9 days until next milestone

First Posted

Study publicly available on registry

June 1, 2026

Completed
Same day until next milestone

Study Start

First participant enrolled

June 1, 2026

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 30, 2026

Expected
21 days until next milestone

Study Completion

Last participant's last visit for all outcomes

November 20, 2026

Last Updated

June 29, 2026

Status Verified

April 1, 2026

Enrollment Period

5 months

First QC Date

May 23, 2026

Last Update Submit

June 25, 2026

Conditions

Keywords

Pain Neuroscience EducationTelerehabilitationSupervised Clinic Based RehabKinesiophobiaChronic Non-Specific Neck Pain

Outcome Measures

Primary Outcomes (3)

  • Numeric Pain Rating Scale for Pain Intensity (NPRS)

    Pain intensity will be assessed using the Numeric Pain Rating Scale (NPRS), an 11-point self-reported scale ranging from 0 (no pain) to 10 (worst imaginable pain). The NPRS is a valid, reliable, and responsive tool commonly used to evaluate pain intensity in individuals with neck pain.

    6 weeks

  • Neck Disability Index for Functional Disability (NDI)

    Functional disability will be assessed using the Neck Disability Index (NDI), a self-reported questionnaire consisting of 10 items related to daily activities, including pain intensity, personal care, lifting, reading, concentration, headache, work, driving, sleeping, and recreation. Each item is scored from 0 to 5, with total scores ranging from 0 to 50. Higher scores indicate greater disability.

    6 weeks

  • Tampa Scale of Kinesiophobia (TSK-11)

    Kinesiophobia will be assessed using the 11-item Tampa Scale of Kinesiophobia (TSK-11). Each item is scored on a 4-point Likert scale ranging from 1 (strongly disagree) to 4 (strongly agree), with total scores ranging from 11 to 44. Higher scores indicate greater fear of movement and reinjury.

    6 weeks

Study Arms (2)

Telerehabilitation with Pain Neuroscience Education

EXPERIMENTAL

Participants will receive a structured rehabilitation program delivered via online platforms. The intervention includes therapeutic exercises targeting cervical and scapular muscles along with pain neuroscience education. Sessions will be conducted three times per week for six weeks under remote supervision.

Other: Telerehabilitation with Pain Neuroscience Education

Supervised Clinic Based Rehab with Pain Neuroscience Education

ACTIVE COMPARATOR

Participants will receive supervised face-to-face physiotherapy in a clinical setting. The intervention includes the same therapeutic exercises and pain neuroscience education as the experimental group, delivered under direct supervision of a physiotherapist. Sessions will be conducted three times per week for six weeks.

Other: Supervised Clinic Based Rehab with Pain Neuroscience Education

Interventions

A remotely delivered physical therapy program including stretching and strengthening exercises for cervical and scapular muscles combined with pain neuroscience education, delivered via online platforms three times per week for six weeks.

Telerehabilitation with Pain Neuroscience Education

A clinic-based physiotherapy program including stretching and strengthening exercises for cervical and scapular muscles combined with pain neuroscience education, delivered under direct supervision three times per week for six weeks.

Supervised Clinic Based Rehab with Pain Neuroscience Education

Eligibility Criteria

Age18 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Age between 18-40 years of both male and female gender.
  • Currently suffering from neck pain \& bilateral neck pain for at least three months.
  • Moderate pain intensity (30mm to 70mm) on Visual Analogue Scale .
  • Access \& knowledge of mobile phone and internet use .

You may not qualify if:

  • Any previous neck surgery or cervical trauma .
  • Fibromyalgia \& Myelopathy .
  • Spinal deformities like thoracic hyper kyphosis or scoliosis .
  • Cervical radiculopathy ,vertigo, cancer \& vertebral fractures.
  • Infection or inflammatory arthritis in cervical spine .
  • History of the whiplash injury .
  • Physiotherapeutic treatment in the last six months .
  • Cognitive disorder that prohibited the pain neuroscience education intervention from being followed .

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Saleem Memorial Hospital Lahore

Lahore, 54000, Pakistan

RECRUITING

MeSH Terms

Conditions

Kinesiophobia

Interventions

Telerehabilitation

Condition Hierarchy (Ancestors)

Phobic DisordersAnxiety DisordersMental Disorders

Intervention Hierarchy (Ancestors)

RehabilitationAftercareContinuity of Patient CarePatient CareTherapeuticsHealth ServicesHealth Care Facilities Workforce and ServicesTelemedicineDelivery of Health CarePatient Care ManagementHealth Services Administration

Study Officials

  • Dr Shoaib Waqas, Phd

    Lahore University of Biological and Applied Sciences

    STUDY DIRECTOR

Central Study Contacts

Dr Shoaib Waqas, Phd

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

May 23, 2026

First Posted

June 1, 2026

Study Start

June 1, 2026

Primary Completion (Estimated)

October 30, 2026

Study Completion (Estimated)

November 20, 2026

Last Updated

June 29, 2026

Record last verified: 2026-04

Locations