Skip to content

Effects of Kendall Exercise Versus Gong's Mobilization in Text Neck Syndrome. A Pilot Study

Effects of Kendall Exercise Versus Gong's Mobilization on Pain, Range of Motion, Function and Strength in Text Neck Syndrome. A Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04813315
Enrollment
12
Registered
2021-03-24
Start date
2019-10-15
Completion date
2021-04-15
Last updated
2022-07-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neck Pain

Keywords

neck pain

Brief summary

This project was a pilot randomized trial conducted to compare the effects of Kendall exercise and Gong's mobilization on pain, range of motion, function and strength in text neck syndrome so that we can have best treatment option for patients with neck pain

Detailed description

Non Probability Convenient sampling was done. Patients following eligibility criteria from Fatima hospital Sargodha were considered. Sample size was calculated 12. Participants were randomly allocated in two groups equally via convenient sampling method. Baseline assessment was done initially. Group A was given Kendall exercise and Group B was given Gong's mobilization along with conventional physiotherapy treatment (hot pack). Duration of research was almost 6 months. Participants were treated 3 times a week for 4 weeks. Pre and Post treatment readings were taken in 1st session and 4th week period respectively. Assessment was done via Numeric pain rating scale (NPRS),Neck Disability index (NDI), Universal goniometer and Modified sphygmomanometer test. All participants were provided written informed consent prior to commencement of the procedures. They were free to quit the treatment at any stage of research. Data was analyzed by using SPSS version 23.

Interventions

consist of stretch of pectoralis major and neck extensor strengthening of deep neck flexors and scapular retractor

it is combination of glide along the facet joint and concurrent movement of cervical spine

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* Young adults * more than one year using a smartphone * Using smart phone for more than 2 hours a day * Craniovertebral angle(CVA)less than 53° * Score of more than 3 on NPRS and more than 10 on NDI

Exclusion criteria

* Spinal infection or inflammatory disorder * Neck surgery or trauma * Torticollis, scoliosis * Malignancy, pregnancy * Diagnosed cases of disc prolapse, stenosis, herniation, spondylolisthesis and osteoporosis * Current use of any medication or physical therapy treatment.

Design outcomes

Primary

MeasureTime frameDescription
Numeric pain rating scale4th weekNumeric pain rating scale range from 0-10, 0 means no pain- 10 means severe pain First checked at baseline and than 4th week
Range of Motion4th weekAll ranges of neck: 80° to 90° of flexion, 70° of extension, 20° to 45° of lateral flexion, and up to 90° of rotation to both sides. All ranges other than the written will be considered abnormal. First checked at baseline and than 4th week
Neck Disability Index4th weekEach of the 10 items is scored from 0 - 5. The maximum score is therefore 50. o means no pain 5 means maximum pain Each of the 10 items is scored from 0 - 5. The maximum score is therefore 50.0 means no disability, 50 means full limitation.A higher score indicates more patient-rated disability. First checked at baseline and than 4th week
Modified Sphygmomanometer test4th weekIt is used to measure strength of muscles. change in 2mm cause minimal detectable change. First checked at baseline and than 4th week

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026