Comparison of Gongs and Kaltenborn Mobilization on Neck Pain
Comparison of Gongs Mobilization and Kaltenborn Mobilization on Mechanical Neck Pain
1 other identifier
interventional
44
1 country
1
Brief Summary
The aim of this randomized controlled trial is to find the effect of Gongs mobilization in comparison with Kaltenborn mobilization on mechanical neck pain , range of motion and proprioception.A randomized control trial that will include total 44 participants. The first group will receive Gongs mobilization along with conventional therapy and 2nd group will receive Kaltenborn mobilization along with conventional therapy.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Aug 2024
Shorter than P25 for not_applicable
1 active site
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
Study Start
First participant enrolled
August 9, 2024
CompletedFirst Submitted
Initial submission to the registry
August 13, 2024
CompletedFirst Posted
Study publicly available on registry
August 16, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
January 10, 2025
CompletedAugust 16, 2024
August 1, 2024
5 months
August 13, 2024
August 13, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Numeric Pain Rating Scale NPRS
The NPRS is a segmented numeric version of the visual analog scale which is used to assess pain. It scores ranges from 0-10, 0 means No pain and 10 means Severe pain. Patient will be asked to verbally report the pain score.
4 weeks
Secondary Outcomes (2)
: Goniometer
4 weeks
Cervical Joint Position Error
4 weeks
Study Arms (2)
Group A
EXPERIMENTALGongs mobilization and conventional therapy , sessions 3 per week , mobilization for 5 minutes and 30 minutes session for total 4 weeks. exercise 3 sets for 10 repetitions. Modality (Hydrocollator pack, TENS for 15 minutes with pulse frequency of 10-200 Hz, pulse width 100 - 250 micro seconds.
Group B
EXPERIMENTALKaltenborn mobilization along with cervical traction and conventional therapy: Intervention will be given 3 times/week 5 minutes mobilization Exercise 3 sets for 10 repetitions and 30 minutes session for 4 consecutive weeks. Modality including (Hydrocollator pack, TENS for 15 minutes with pulse frequency of 10-200 Hz, pulse width 100 - 250 micro seconds. Intensity tolerated by patients.
Interventions
3 per week , mobilization for 5 minutes , exercise 3 sets for 10 repetitions for 4 consecutive weeks
3 per week , mobilization for 5 minutes , exercise 3 sets for 10 repetitions for 4 consecutive weeks.
Eligibility Criteria
You may qualify if:
- Participants falling in this category would be recruited into the study.
- Age 18 -65 years
- Both male and female
- Primary complaint of neck pain with or without radiating to Upper extremity
- Pain confined to posterior aspect of neck with mechanical characteristics such as symptoms provoked by neck movement, by palpation of cervical muscles and by sustained posture.
- Subjects who are willing to participate in study.
- Patients with Mechanical neck pain
You may not qualify if:
- Participants falling in this category would be excluded from the study.
- Bilateral upper extremity symptoms
- Whiplash injury
- Trauma or tumor around neck
- Previous neck surgery
- Spinal infection
- Cervical radiculopathy and myelopathy
- Vascular syndromes
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Alam Hospital Attock
Attock City, Punjab Province, 43350, Pakistan
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Madiha Ali, MS OMPT
Riphah International University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 13, 2024
First Posted
August 16, 2024
Study Start
August 9, 2024
Primary Completion
December 30, 2024
Study Completion
January 10, 2025
Last Updated
August 16, 2024
Record last verified: 2024-08
Data Sharing
- IPD Sharing
- Will not share