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

Not Applicable
Completed
Conditions
Neck Pain
Interventions
Other: Gong's mobilization
Other: Kendall exercise
Registration Number
NCT04813315
Lead Sponsor
Riphah International University
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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
12
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
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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.
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Gong's mobilizationGong's mobilizationExperimental group 1 got this intervention containing Gong's mobilization for 15-20 mins, followed by conventional physiotherapy treatment (hot pack).Participants were treated 3 times per week for 4 weeks. Pre and Post treatment readings were taken in 1st session and 4th week respectively. Assessment was done via Numeric pain rating scale, neck disability index, universal goniometer and modified sphygmomanometer test.
Kendall exerciseKendall exerciseExperimental group 1 got this intervention containing Kendall exercise for 15-20 mins, followed by conventional physiotherapy treatment (hot pack).Participants were treated 3 times per week for 4 weeks. Pre and Post treatment readings were taken in 1st session and 4th week respectively. Assessment was done via Numeric pain rating scale, neck disability index, universal goniometer and modified sphygmomanometer test.
Primary Outcome Measures
NameTimeMethod
Range of Motion4th week

All 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 week

Each 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 week

It is used to measure strength of muscles. change in 2mm cause minimal detectable change.

First checked at baseline and than 4th week

Numeric pain rating scale4th week

Numeric pain rating scale range from 0-10, 0 means no pain- 10 means severe pain First checked at baseline and than 4th week

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Riphah IU

🇵🇰

Lahore, Punjab, Pakistan

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