Effects of Telerehabilitation and Supervised Clinic Based Rehab With Pain Neuroscience Education for Pain,Kinesiophobia and Functional Disability Among Chronic Non-Specific Neck Pain Patients
1 other identifier
interventional
45
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jun 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 23, 2026
CompletedFirst Posted
Study publicly available on registry
June 1, 2026
CompletedStudy Start
First participant enrolled
June 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
November 20, 2026
June 29, 2026
April 1, 2026
5 months
May 23, 2026
June 25, 2026
Conditions
Keywords
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
EXPERIMENTALParticipants 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.
Supervised Clinic Based Rehab with Pain Neuroscience Education
ACTIVE COMPARATORParticipants 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.
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.
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.
Eligibility Criteria
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
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Dr Shoaib Waqas, Phd
Lahore University of Biological and Applied Sciences
Central Study Contacts
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