Effects of a Wearable Device ,Phone App and Exercise on Cervico-thoracic Posture in University Students.

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-30
SponsorRiphah International University

About this trial

Forward head posture and thoracic kyphosis are among the most common postural problems in university students, driven largely by long hours of screen use and poor sitting habits. Research suggests that nearly two-thirds of university students show measurable forward head posture, and if uncorrected, it is linked to chronic neck pain and long-term musculoskeletal strain. This study compares three approaches to correcting posture over a six-week supervised exercise program: a wearable sensor belt that vibrates in real time when posture slips, a smartphone app that sends scheduled reminders throughout the day, and exercise alone with no reminders. The two technology-assisted groups are prompted to correct their posture throughout daily activities, not just during exercise sessions. The study will show whether real-time or scheduled reminders produce greater improvements in posture, neck pain, and neck function than exercise alone . Helping physical therapists and university health services to identify the most practical strategy for correcting posture in screen-heavy academic environments.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

University students aged 18-30 years enrolled in a degree program at Riphah International University.

Daily sitting duration ≥ 5 hours (academic and/or device-related activities).

Presence of at least one observable postural deviation confirmed at baseline assessment: forward head posture (CVA < 50°), rounded shoulders (protracted shoulder distance in supine line), or thoracic kyphosis (> 40° via digital inclinometer).

Smartphone ownership and basic digital literacy

Disqualifiers

History of spinal surgery, vertebral fracture, or major cervical/thoracic trauma within the past 12 months.

Diagnosed neurological disorders affecting posture or motor control (e.g., Parkinson's disease, stroke, cervical dystonia).

Structural spinal deformities requiring active medical or surgical management (e.g., scoliosis Cobb angle > 20°, Scheuermann's kyphosis).

Current participation in physiotherapy, chiropractic treatment, or another structured posture correction program.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Wearable postural biofeedback device

    Device

    A wearable belt worn around the cervicothoracic region that detects postural deviation in real time and provide vibratory feedback to prompt immediate self-correction , used in conjunction with standardized exercise program.

  • App based Postural Reminder

    Behavioral

    A smartphone application that delivers scheduled reminders prompting participants to self-check and correct their posture throughout the day, used in conjunction with the standardized exercise program

  • Conventional Cervicothoracic Exercise Therapy

    Other intervention

    A structured , supervised exercise program targeting cervicothoracic postural muscles , delivered without any wearable device or app based reminder

Treatment groups

87 Participants
are divided into 3 treatment groups
Group A: Wearable Device + ExerciseExperimental treatment 1 intervention
Group B: App- based Reminder + ExerciseExperimental treatment 1 intervention
Group C: Conventional Exercise TherapyActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Change in Craniovertebral angle

Degree of forward head posture measured via photogrammetry app, Calculated as angle between a horizontal line through C7 and a line to tragus of the ear. Normal CVA is greater than 50 degrees.

Time frame
baseline ,Mid treatment (4th week) , Post intervention (6th week) and follow up (12th week)
2

Thoracic Kyphosis Angle

Degree of thoracic spinal curvature (T1 - T12) measured using a digital inclinometer. Normal range 20 degree to 45 degree

Time frame
At Baseline , Mid treatment Intervention (4th week) , Post intervention (6th week) and follow up at 12 week

Secondary outcomes

1

Change in Neck Disability Index Score

10 item self report questionnaire assessing functional disability related neck pain . Score converted to percentage ,higher score means greater disability. Excellent test re test reliability ,ICC score of 0.91

Time frame
At Baseline , Mid intervention (4th week) , Post Intervention (6th week ) and follow up at 12th week
2

Change in Neck and Upper Back Pain Intensity

Subjective pain intensity rated on NPRS ,an 11-point scale (0 = no pain, 10 = worst pain imaginable).The test retest reliability range from 0.67 - 0.96

Time frame
At Baseline , Mid intervention (4th week) , Post Intervention (6th week) and follow up at 12 week.
3

Change in Shoulder Protraction Distance

Horizontal distance from the posterolateral acromion to a table surface, measured with participant supine (Table Top Test). Distance greater than 2.6 cm indicates protracted shoulder posture.

Time frame
At Baseline , Mid intervention (4th week) , Post Intervention (6th week) and follow up at 12 week.
4

Change in Postural Awareness Scale Score.

12-item validated self-report questionnaire assessing postural awareness and body perception, scored 12-60. Higher scores indicate better awareness. The test retest reliability value (ICC) is 0.75-0.83

Time frame
At Baseline , Mid intervention (4th week) , Post Intervention (6th week) and follow up at 12 week

Other outcomes

1

Intervention Adherence Rate

Session attendance, exercise completion rate, and app/wearable device usage recorded via attendance registers, digital app logs, and wearable device session records, depending on group assignment.

Time frame
At Baseline , Mid intervention (4th week) , Post Intervention (6th week) and follow up at 12 week.

Sponsors and contacts

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