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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-35
SponsorLahore University of Biological and Applied Sciences

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

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

Trial design

Design model

Parallel

Treatments tested in this trial

  • Neck and upper back strengthening exercises by Tele-rehabilitation Intervention

    Other 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.

  • Neck and upper back strengthening by Supervised Rehabilitation Intervention

    Other 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.

Treatment groups

62 Participants
are divided into 2 treatment groups
Group A: Telerehabilitation GroupExperimental treatment 1 intervention
Group B: Supervised Rehabilitation GroupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Neck Pain

Neck 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".

Time frame
From enrollment to the end of treatment at 8 weeks

Secondary outcomes

1

Disability

The 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.

Time frame
From enrollment to the end of treatment at 8 weeks
2

Exercise Adherence

Exercise 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.

Time frame
From enrollment to the end of treatment at 8 weeks

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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