NCT07163533

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
64

participants targeted

Target at P50-P75 for not_applicable

Timeline
2mo left

Started Feb 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

2 active sites

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress62%
Feb 2026Jul 2026

First Submitted

Initial submission to the registry

September 1, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

September 9, 2025

Completed
5 months until next milestone

Study Start

First participant enrolled

February 1, 2026

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

July 30, 2026

Last Updated

March 30, 2026

Status Verified

March 1, 2026

Enrollment Period

5 months

First QC Date

September 1, 2025

Last Update Submit

March 25, 2026

Conditions

Keywords

Forward head posture (FHP)Vibrotactile feedback sensorsKendall exercisesCraniovertebral angleInertial measure units

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 )

EXPERIMENTAL

this group will receives wearable sensors plus Kendall exercises for 4 weeks

Other: wearble vibrotactile feedback sensor and kendel exercises

group B (kendall exercises only )

ACTIVE COMPARATOR

this group will receives Kendall exercises for 4 weeks

Other: kendel exercises

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.

group B (kendall exercises only )

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.

group A ( wearable sensors plus kendall exercises )

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

NOT YET RECRUITING

Margalla institute of health sciences

Rawalpindi, Punjab Province, 46000, Pakistan

RECRUITING

MeSH Terms

Conditions

Neck Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • aisha razzaq, PHD

    Riphah International University

    PRINCIPAL INVESTIGATOR

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

Locations