Effect of Myofascial Release Therapy on University Students With Text Neck Syndrome.

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-30
SponsorUniversity of Health Sciences Lahore

About this trial

This randomized controlled trial aims to determine the effectiveness of myofascial release therapy in university students with text neck syndrome as prolonged smartphone and digital gadgets use has been associated with neck pain, forward head posture, and increased perceived stress among young adults with screen time more than 3 hours. Participants will be randomly allocated into control group and intervention group and will be treated for 4 weeks. Clinical outcomes including neck pain, neck pain intensity, craniovertebral angle for posture assessment, and perceived stress levels will be measured at baseline and post-intervention. The study seeks to determine whether Myofascial Release Therapy acts as a non-invasive technique in improving musculoskeletal and psychosocial parameters related to text neck.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

1. university students from age group of 18-30 2. Both genders 3. Students with Text Neck Syndrome diagnosed via Forward head Posture (through measuring craniovertebral angle) <50° 4. Minimum Pain measured by Visual Analog Scale (VAS) ≥ 3/10 5. Pain Intensity measured through Neck Disability Index (NDI > 10%) 6. A PSS-10 Score of >14 in individuals with daily gadget use and FHP. 7. Usage of handheld digital gadgets including smartphones and tablets ≥ 3 hours

Disqualifiers

1. History of cervical trauma, surgery or any spine deformity which is congenital 2. History of diagnosed cervical disorders i.e cervical spondylosis, cervical spondylolisthesis, disc herniation 3. Any diagnosed neurological condition which affects cognition or any previous cervical spine surgery 4. Any history of diagnosed anxiety and psychiatric conditions 5. Currently receiving any form of physical therapy or using any muscle relaxants or painkillers

Trial design

Design model

Parallel

Treatments tested in this trial

  • Myofascial Release Therapy

    Behavioral

    Participants will receive Myofascial Release Therapy targeting neck and upper back muscles, 3 sessions per week for 4 weeks. This is a physical therapy intervention.

  • Standard Care (Treatment as Usual)

    Behavioral

    Participants will receive conventional physiotherapy including postural correction exercises, stretching of neck and upper back muscles, and ergonomic education. Outcomes will be measured after the intervention.

Treatment groups

62 Participants
are divided into 2 treatment groups
Group A: InterventionExperimental treatment 2 interventions
Group B: Conventional Physical TherapyActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Neck Pain

Neck pain will be assessed using the Visual Analog Scale (VAS), where participants rate their pain intensity on a scale from 0 (no pain) to 10 (worst imaginable pain)

Time frame
Baseline and after 4 weeks of intervention
2

Perceived Stress

Perceived stress will be assessed using the Perceived Stress Scale (PSS), a validated questionnaire measuring the degree to which situations in one's life are appraised as stressful.

Time frame
Baseline and after 4 weeks of intervention
3

Forward Head Posture

Forward Head Posture will be measured using the craniovertebral angle (CVA) from lateral photographs using Kinovea Software. A smaller angle indicates a more pronounced forward head posture.

Time frame
Baseline and after 4 weeks

Secondary outcomes

Other outcomes

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