NCT06556771

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

57
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
44

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Aug 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

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 Start

First participant enrolled

August 9, 2024

Completed
4 days until next milestone

First Submitted

Initial submission to the registry

August 13, 2024

Completed
3 days until next milestone

First Posted

Study publicly available on registry

August 16, 2024

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2024

Completed
11 days until next milestone

Study Completion

Last participant's last visit for all outcomes

January 10, 2025

Completed
Last Updated

August 16, 2024

Status Verified

August 1, 2024

Enrollment Period

5 months

First QC Date

August 13, 2024

Last Update Submit

August 13, 2024

Conditions

Keywords

Gongs mobilization, Kaltenborn mobilization , Mechanical neck pain , proprioception

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

EXPERIMENTAL

Gongs 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.

Other: Gongs mobilization + conventional physical therapy

Group B

EXPERIMENTAL

Kaltenborn 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.

Other: Kaltenborn mobilization along with traction + conventional therapy

Interventions

3 per week , mobilization for 5 minutes , exercise 3 sets for 10 repetitions for 4 consecutive weeks

Group A

3 per week , mobilization for 5 minutes , exercise 3 sets for 10 repetitions for 4 consecutive weeks.

Group B

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

RECRUITING

MeSH Terms

Interventions

Traction

Intervention Hierarchy (Ancestors)

Orthopedic ProceduresSurgical Procedures, Operative

Study Officials

  • Madiha Ali, MS OMPT

    Riphah International University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Madiha Ali, MS-OMPT

CONTACT

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

Locations