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临床试验/NCT07763327
NCT07763327尚未招募不适用

Comparison of Wearable Device -Based , App- Based ,and Conventional Exercise Therapy for Cervico-Thoracic Postural Training in University Students.

Riphah International University1 个研究点 分布在 1 个国家目标入组 87 人开始时间: 2026年8月17日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
87
试验地点
1
主要终点
Change in Craniovertebral angle

研究概览

简要总结

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.

详细描述

Forward head posture(FHP) and thoracic kyphosis are increasingly prevalent among university students due to sustained flexed-neck postures during smartphone use, laptop-based study, and prolonged sitting. Chronic FHP alters the normal cervical lordotic curve, increases mechanical loading on cervical spine structures, and has been associated with muscular imbalance, cervicogenic pain , and headache.

Conventional postural correction exercise programs are well established, but adherence to postural correction outside of supervised sessions remains a key limitation. Students are typically unaware of their posture lapsing during daily activities such as studying, phone use and prolonged sitting and correction cues are usually absent outside the clinical or exercise setting.

Technology-assisted feedback systems have emerged as a potential solution to this adherence gap. Wearable biofeedback devices provide immediate, real-time correction cues when a threshold postural deviation is detected, theoretically reinforcing correct postural habits through continuous behavioral conditioning. App-based reminder systems, offers a scheduled, intermittent prompts rather than continuous monitoring , it is more practical and scalable given lower cost and no specialized hardware requirement.

This three arm, parallel group randomized controlled trial is designed to generate comparative evidence on the relative effectiveness of continuous biofeedback, scheduled reminders, and conventional exercise therapy alone, in order to inform evidence-based, resource-appropriate postural correction strategies for university and academic health settings.

The results of this trial are intended to directly inform clinical decision-making for physiotherapists and university wellness programs considering adoption of wearable or app-based postural correction tools. Should either technology-assisted approach demonstrate superiority over conventional exercise alone, this would support integration of low-cost, scalable postural feedback technology into standard student musculoskeletal health programs. Conversely, if outcomes are comparable across groups, this would support conventional supervised exercise as a sufficient, lower-cost first-line approach, without the added expense or complexity of technology-assisted feedback devices.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 30 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •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

排除标准

  • •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.
  • •Cardiovascular or pulmonary conditions contraindicating moderate-intensity exercise (e.g., uncontrolled hypertension, severe asthma).
  • •Skin conditions, open wounds, or allergies precluding safe use of the posture correction belt.

研究组 & 干预措施

Wearable Device + Exercise

Experimental

Participants will receive a wearable biofeedback belt that provides real time vibration feedback upon postural deviation, in addition to the standardized cervicothoracic exercise program administered to all groups , over a 6 week intervention period

干预措施: Wearable postural biofeedback device (Device)

App- based Reminder + Exercise

Experimental

Participants will receive scheduled posture-check reminders via a smartphone application, in addition to the standardized cervicothoracic exercise program administered to all groups , over a 6 week intervention period.

干预措施: App based Postural Reminder (Behavioral)

Conventional Exercise Therapy

Active Comparator

Participants will receive the standardized cervicothoracic exercise program alone over a 6 week intervention period, without any wearable device or app based reminder.

干预措施: Conventional Cervicothoracic Exercise Therapy (Other)

结局指标

主要结局

Change in Craniovertebral angle

时间窗: baseline ,Mid treatment (4th week) , Post intervention (6th week) and follow up (12th week)

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.

Thoracic Kyphosis Angle

时间窗: At Baseline , Mid treatment Intervention (4th week) , Post intervention (6th week) and follow up at 12 week

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

次要结局

  • Change in Neck Disability Index Score(At Baseline , Mid intervention (4th week) , Post Intervention (6th week ) and follow up at 12th week)
  • Change in Neck and Upper Back Pain Intensity(At Baseline , Mid intervention (4th week) , Post Intervention (6th week) and follow up at 12 week.)
  • Change in Shoulder Protraction Distance(At Baseline , Mid intervention (4th week) , Post Intervention (6th week) and follow up at 12 week.)
  • Change in Postural Awareness Scale Score.(At Baseline , Mid intervention (4th week) , Post Intervention (6th week) and follow up at 12 week)
  • Change in Deep Neck Flexor Muscle Endurance(At Baseline , Mid intervention (4th week) , Post Intervention (6th week) and follow up at 12 week)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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