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

2026年8月10日 更新者:Riphah International University

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

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.

調査の概要

詳細な説明

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.

University students represent a population with high daily screen-time exposure and sedentary study behavior, making them broadly representative of the wider demographic at risk for posture-related cervical musculoskeletal strain seen in academic and early-career professional environments. Evidence generated from this population is expected to have relevance beyond the immediate study setting, informing postural health strategies applicable to similarly screen-intensive occupational and educational contexts.

研究の種類

介入

入学 (推定)

87

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

      • Islamabad、パキスタン、44000
        • Postgraduation Lab of Riphah College of Rehabilitation & Allied Health Sciences , Riphah International University. Islamabad
        • コンタクト:
        • 主任研究者:
          • Huma Riaz, PhD

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  1. University students aged 18-30 years enrolled in a degree program at Riphah International University.
  2. Daily sitting duration ≥ 5 hours (academic and/or device-related activities).
  3. 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).
  4. Smartphone ownership and basic digital literacy

Exclusion Criteria:

  1. History of spinal surgery, vertebral fracture, or major cervical/thoracic trauma within the past 12 months.
  2. Diagnosed neurological disorders affecting posture or motor control (e.g., Parkinson's disease, stroke, cervical dystonia).
  3. Structural spinal deformities requiring active medical or surgical management (e.g., scoliosis Cobb angle > 20°, Scheuermann's kyphosis).
  4. Current participation in physiotherapy, chiropractic treatment, or another structured posture correction program.
  5. Cardiovascular or pulmonary conditions contraindicating moderate-intensity exercise (e.g., uncontrolled hypertension, severe asthma).
  6. Skin conditions, open wounds, or allergies precluding safe use of the posture correction belt.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:独身

武器と介入

参加者グループ / アーム
介入・治療
実験的:Wearable Device + Exercise
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
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.
実験的:App- based Reminder + Exercise
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.
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
アクティブコンパレータ:Conventional Exercise Therapy
Participants will receive the standardized cervicothoracic exercise program alone over a 6 week intervention period, without any wearable device or app based reminder.
A structured , supervised exercise program targeting cervicothoracic postural muscles , delivered without any wearable device or app based reminder

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Change in Craniovertebral angle
時間枠: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.
baseline ,Mid treatment (4th week) , Post intervention (6th week) and follow up (12th week)
Thoracic Kyphosis Angle
時間枠: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
At Baseline , Mid treatment Intervention (4th week) , Post intervention (6th week) and follow up at 12 week

二次結果の測定

結果測定
メジャーの説明
時間枠
Change in Neck Disability Index Score
時間枠:At Baseline , Mid intervention (4th week) , Post Intervention (6th week ) and follow up at 12th week
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
At Baseline , Mid intervention (4th week) , Post Intervention (6th week ) and follow up at 12th week
Change in Neck and Upper Back Pain Intensity
時間枠:At Baseline , Mid intervention (4th week) , Post Intervention (6th week) and follow up at 12 week.
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
At Baseline , Mid intervention (4th week) , Post Intervention (6th week) and follow up at 12 week.
Change in Shoulder Protraction Distance
時間枠:At Baseline , Mid intervention (4th week) , Post Intervention (6th week) and follow up at 12 week.
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.
At Baseline , Mid intervention (4th week) , Post Intervention (6th week) and follow up at 12 week.
Change in Postural Awareness Scale Score.
時間枠:At Baseline , Mid intervention (4th week) , Post Intervention (6th week) and follow up at 12 week
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
At Baseline , Mid intervention (4th week) , Post Intervention (6th week) and follow up at 12 week
Change in Deep Neck Flexor Muscle Endurance
時間枠:At Baseline , Mid intervention (4th week) , Post Intervention (6th week) and follow up at 12 week
Endurance capacity of deep cervical flexor muscles (longus colli, longus capitis), measured in seconds using the Deep Neck Flexor Endurance Test. With good Intra rater Reliability (ICC= 0.81 - 0.94)
At Baseline , Mid intervention (4th week) , Post Intervention (6th week) and follow up at 12 week

その他の成果指標

結果測定
メジャーの説明
時間枠
Intervention Adherence Rate
時間枠:At Baseline , Mid intervention (4th week) , Post Intervention (6th week) and follow up at 12 week.
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.
At Baseline , Mid intervention (4th week) , Post Intervention (6th week) and follow up at 12 week.

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

捜査官

  • 主任研究者:Huma Riaz, PhD、Riphah International University, Islamabad

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年8月17日

一次修了 (推定)

2027年6月30日

研究の完了 (推定)

2027年7月31日

試験登録日

最初に提出

2026年8月10日

QC基準を満たした最初の提出物

2026年8月10日

最初の投稿 (実際)

2026年8月13日

学習記録の更新

投稿された最後の更新 (実際)

2026年8月13日

QC基準を満たした最後の更新が送信されました

2026年8月10日

最終確認日

2026年8月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

IPD プランの説明

No formal data sharing infrastructure exists for this single site academic thesis study. De-identified individual participant data may be shared upon reasonable request to the corresponding investigator , subject to institutional approval from Riphah International University.

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米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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