Actively Recruiting

Phase Not Applicable
Age: 18Years - 30Years
All Genders
NCT07163533

Combined Effect of Kendall Exercises With Wearable Vibrotactile Feedback Sensor in Forward Head Posture

Led by Riphah International University · Updated on 2026-03-30

64

Participants Needed

2

Research Sites

25 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of this research is to determines Combined Effect of Kendall exercises with Wearable vibrotactile feedback Sensor on Forward Head Posture correction on neck pain, and improving craniovertebral angle and muscle thickness. Randomized controlled trials at Fauji Foundation Hospital and Margalla Institute of health sciences . The sample size was 64. The subjects were divided in two groups, 32 subjects will be included in wearbable sensors and kendall exercises group and 32 will be in Kendell exercise alone . Study duration will be 12 months. Sampling technique applied will be non probability convinience sampling technique. Participants eligible for recruitment in this study will include young adults between the ages of 18 and 30 years. Eligible participants must also present with a craniovertebral angle (CVA) of less than 50 degrees, a body mass index (BMI) within the range of 18.5-30 kg/m², and a daily screen time of less than five hours. Data will be analyzed through SPSS version 26.

CONDITIONS

Official Title

Combined Effect of Kendall Exercises With Wearable Vibrotactile Feedback Sensor in Forward Head Posture

Who Can Participate

Age: 18Years - 30Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Young adult aged between 18 to 30 years
  • Both genders eligible
  • Craniovertebral angle (CVA) less than 50 degrees
  • Body mass index (BMI) between 18.5 and 30 kg/m2
  • Dentists with more than 6 months of clinical experience
Not Eligible

You will not qualify if you...

  • History of neck or spinal surgery within the past 6 to 12 months
  • Musculoskeletal, neurological, or vestibular disorders affecting posture or neck movement
  • Diagnosed temporomandibular dysfunction
  • Use of assistive devices like neck braces or posture correctors in the past 3 months
  • Cognitive or psychological conditions affecting compliance or symptom reporting
  • Currently participating in exercise or physiotherapy programs targeting posture or neck muscles

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Foundation University School of Health Sciences

Rawalpindi, Punjab Province, Pakistan, 44000

Not Yet Recruiting

2

Margalla institute of health sciences

Rawalpindi, Punjab Province, Pakistan, 46000

Actively Recruiting

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Research Team

I

Imran Amjad, PHD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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