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Effects of Tele-rehabilitation Versus Supervised Rehabilitation Among Computer Users With Non-specific Neck Pain

Effects of Tele-rehabilitation Versus Supervised Rehabilitation on Neck Pain, Disability and Exercise Adherence Among Computer Users With Non-specific Neck Pain: A Randomized Controlled Trial

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07556705
Enrollment
62
Registered
2026-04-29
Start date
2026-05-01
Completion date
2026-09-01
Last updated
2026-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non Specific Neck Pain

Keywords

Neck pain, Telerehabilitation, Supervised exercise therapy, Computer users, Exercise adherence, Musculoskeletal pain assessment tool

Brief summary

The current study is a single-blinded, two-arm parallel-group randomized controlled trial involving 62 participants with non-specific neck pain among computer users. The trial aims to compare the effects of tele-rehabilitation and supervised rehabilitation on neck pain, disability, and exercise adherence. Both groups will receive the same structured exercise program along with postural correction instructions. The tele-rehabilitation group will perform exercises remotely with digital guidance, reminders, and follow-ups, while the supervised group will receive in-clinic physiotherapy sessions under professional supervision. Interventions will be carried out three times per week for a duration of six weeks, with each session lasting approximately 40 minutes. Outcome measures will include neck pain (VAS), neck disability (NDI), and exercise adherence (ATEMPT tool).Assessments will be conducted at baseline and at the end of treatment at 8th week.The study will be conducted at the Physical Therapy Department of Sehat Medical Complex Lake City, and the University of Lahore Teaching Hospital. The hypothesis is that tele-rehabilitation will be more effective than supervised rehabilitation in reducing neck pain and disability, and may result in better exercise adherence due to its convenience and accessibility.

Detailed description

Non-specific neck pain (NSNP) is a significant medical and socioeconomic issue, particularly among computer users who maintain prolonged static postures. For these professionals, time poverty due to hectic schedules serves as a primary barrier to recovery and exercise adherence. While conventional supervised rehabilitation is effective, it often requires frequent in-person visits that can limit accessibility. This study will evaluate the effectiveness of a tele-rehabilitation delivery model compared to traditional supervised care in improving neck pain, disability, and exercise adherence. The research uses a single-blinded, two-arm, parallel-group randomized clinical trial design. Tele-rehabilitation Group (TG): Participants receive a digital postural instruction chart and a structured exercise program. Adherence is reinforced through daily WhatsApp notifications and monitored via digital confirmations. Supervised Rehabilitation Group (SG): Participants receive the same exercise protocol and postural instructions but under the direct supervision of a qualified physiotherapist at a clinic. Both interventions are conducted three times a week for 6 weeks, with each session lasting approximately 30 minutes. The study will target 62 computer users aged 18-35 who work more than 35 hours per week and have experienced neck pain for at least 12 weeks. Assessments will be conducted at baseline and every two weeks using the Visual Analogue Scale (VAS) for pain, the Neck Disability Index (NDI), and the Adherence To Exercise for Musculoskeletal Pain Tool (ATEMPT). The study aims to validate a clinic-to-desk model that eliminates geographical and time constraints, potentially reducing work absenteeism and improving the long-term health of the workforce.

Interventions

OTHERNeck and upper back strengthening exercises by Tele-rehabilitation Intervention

Interventions (Postural Awareness, Neck and Upper Back strengthening exercises via Whatsapp reminders).Although both neck and upper back strengthening exercises have demonstrated potential effects individually, there is a paucity of research evaluating their combined effects. A structured program combining both exercises may produce improvements in pain, disability and greater exercise adherence rates when delivered digitally.

OTHERNeck and upper back strengthening by Supervised Rehabilitation Intervention

Interventions ((Postural Awareness, Neck and Upper Back strengthening exercises under supervision) Participants in this group will receive the same 40 -minute session consisting of same exercises as the tele-rehabilitation group in the clinic under the supervision of a physiotherapist.

Sponsors

Lahore University of Biological and Applied Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* Age 18-35 years. * Neck pain that worsens with movement in at-least one direction * Computer users with neck pain for at-least 12 weeks * Neck pain with Visual Analog score of 3 to 8 out of 10 * Participants with forward head posture (FHP) * Working \>35h per week at a desk or computer in a sedentary manner

Exclusion criteria

* Individuals with any neurological or vascular disease * A history of shoulder or spine injuries or surgeries * Participants with history of regular participation or training programs * Participants with body mass index over 30 * Participants having undergone physical therapy or other medical treatments for neck pain in the previous 6 months

Design outcomes

Primary

MeasureTime frameDescription
Neck PainFrom enrollment to the end of treatment at 8 weeksNeck pain will be assessed using the visual analog scale (VAS). The VAS, widely regarded as one of the most reliable and validated methods for self-reporting pain intensity, uses a 10 cm horizontal line. On this scale, 0 cm indicates "no pain," while 10 cm represents "worst pain".

Secondary

MeasureTime frameDescription
DisabilityFrom enrollment to the end of treatment at 8 weeksThe neck disability level will be determined using the Neck Disability Index (NDI), English version. This self-reporting questionnaire determines the disability index of the cervical spine and its impact on daily activities. The NDI has been validated as an effective evaluative tool for patients with neck pain. Each item is scored out of five (with the 'no disability' response given a score of 0), giving a total score for the questionnaire out of 50. Higher scores represent greater disability.
Exercise AdherenceFrom enrollment to the end of treatment at 8 weeksExercise adherence will be measured by using tool "Adherence To Exercise for Musculoskeletal Pain Tool (ATEMPT)". It is the first measure of adherence to exercise for MSK pain. ATEMPT is a uni-dimensional measure that contains six items from the six domains of exercise adherence. The 6-item version of the measure (scored 6-30). Each of the 6 items is scored on a 5-point Likert scale: Strongly Disagree = 1, Disagree = 2, Neither Agree nor Disagree = 3, Agree = 4, Strongly Agree = 5. Sum the scores from all 6 items to get a total between 6 (lowest adherence) and 30 (highest adherence). Higher scores (closer to 30) suggest better adherence to exercise, while lower scores (closer to 6) suggest poorer adherence.

Contacts

CONTACTAmmara Shamoon, MSPT
MSPT243030@ubas.edu.pk03000089740
PRINCIPAL_INVESTIGATORMuhammad Tariq Rafiq, PhD

Lahore University of Biological & Applied Sciences

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 30, 2026