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Not yet recruiting NCT07556705

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

No phase Interventional Non Specific Neck Pain

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Neck and upper back strengthening exercises by Tele-rehabilitation Intervention, Neck and upper back strengthening by Supervised Rehabilitation Intervention.
Who it may be relevant to
Registry conditions: Non Specific Neck Pain. Basic parameters: 18 years — 35 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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

  • Other Neck 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.
  • Other Neck 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.

Primary outcome measures

  • Neck Pain [Time frame: From enrollment to the end of treatment at 8 weeks]
Secondary outcome measures (2)
  • Disability [Time frame: From enrollment to the end of treatment at 8 weeks]
  • Exercise Adherence [Time frame: From enrollment to the end of treatment at 8 weeks]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07556705 · UBAS/ERB/26/04/033

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗