Combined Effect of Kendall Exercises With Wearable Vibrotactile Feedback Sensor in Forward Head Posture
1 other identifier
interventional
64
1 country
2
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Feb 2026
Shorter than P25 for not_applicable
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 1, 2025
CompletedFirst Posted
Study publicly available on registry
September 9, 2025
CompletedStudy Start
First participant enrolled
February 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
July 30, 2026
March 30, 2026
March 1, 2026
5 months
September 1, 2025
March 25, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
neck pain
NPRS(0 to 10) 0 means no pain and 10 means severe pain
baseline to fourth week
craniovertebral angle
angulus app to measure CVA
base line to fourth week
Secondary Outcomes (1)
Neck disability index
baseline to 4th week
Study Arms (2)
group A ( wearable sensors plus kendall exercises )
EXPERIMENTALthis group will receives wearable sensors plus Kendall exercises for 4 weeks
group B (kendall exercises only )
ACTIVE COMPARATORthis group will receives Kendall exercises for 4 weeks
Interventions
kendel exercises consisting of Strengthening of Deep Cervical Flexors, Stretching the Cervical Extensors, Strengthening Shoulder Retraction, Stretching the Pectoralis Muscle. each exercise will be given 3 days per week for 30 min each.
Wearable vibrotactile feedback sensor will be applied to the neck for assessment and management and secondly kendel exercises consisting of Strengthening of Deep Cervical Flexors, Stretching the Cervical Extensors, Strengthening Shoulder Retraction, Stretching the Pectoralis Muscle. each exercise will be given 3 days per week for 30 min each.
Eligibility Criteria
You may qualify if:
- Young Adult with age Between 18 to 30 years
- Both gender
- craniovertebral angle (CVA) \< 50 degrees
- BMI 18.5-30 kg/m2
- dentists having clinical experience more than 6 months
You may not qualify if:
- History of recent neck or spinal surgery (within the past 6 12 months).
- Diagnosed musculoskeletal, neurological, or vestibular disorders affecting posture, balance, or neck movement (e.g., cervical radiculopathy, scoliosis, Parkinson's, etc.).
- Diagnosed Temporomandibular dysfunction
- Use of assistive devices (e.g., neck brace, posture correctors) in the past 3 months.
- Any cognitive or psychological condition that may affect compliance with instructions or accurate reporting of symptoms.
- Ongoing participation in a structured exercise or physiotherapy program targeting posture or neck muscles.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Foundation University School of Health Sciences
Rawalpindi, Punjab Province, 44000, Pakistan
Margalla institute of health sciences
Rawalpindi, Punjab Province, 46000, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
aisha razzaq, PHD
Riphah International University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- Single (Outcomes Assessor) no
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 1, 2025
First Posted
September 9, 2025
Study Start
February 1, 2026
Primary Completion (Estimated)
June 30, 2026
Study Completion (Estimated)
July 30, 2026
Last Updated
March 30, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share