NCT06796452

Brief Summary

This study will be a randomized controlled trial.Non-probability convenient sampling will be used to collect the data. Sample size of 44 subjects with age group between 20-45 years will be taken. Data will be collected from the patients having present complaint of nonspecific Neck pain. Outcome measures will be taken using Numeric pain rating scale (NPRS) for pain, Neck Disability Index (NDI), Muscle endurance by Muscle endurance test using stopwatch and Universal Goniometer (GU) for Range of motion. An informed consent will be taken. Subjects will be selected on the basis of inclusion and exclusion criteria and will be equally divided into two groups by random computer generated numbers method. Group A will receive first and second rib mobilization, and Group B will receive conventional treatment. Outcome measures will be measured prior and after 4 weeks. Data will be analyzed by SPSS version 25.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
44

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Mar 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

First Submitted

Initial submission to the registry

January 22, 2025

Completed
6 days until next milestone

First Posted

Study publicly available on registry

January 28, 2025

Completed
1 month until next milestone

Study Start

First participant enrolled

March 1, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2025

Completed
12 days until next milestone

Study Completion

Last participant's last visit for all outcomes

July 13, 2025

Completed
Last Updated

July 15, 2025

Status Verified

July 1, 2025

Enrollment Period

4 months

First QC Date

January 22, 2025

Last Update Submit

July 14, 2025

Conditions

Keywords

Cervical ribsEndurance

Outcome Measures

Primary Outcomes (2)

  • Numerical Pain Rating Scale

    Patient level of pain will be assessed using this scale by interview method. This scale ranges from 0 to 10. 0 indicates "no pain" and 10 indicates "worst pain".

    4 weeks

  • Universal Goniometer

    The range of motion will be measured using universal goniometer

    4 weeks

Secondary Outcomes (2)

  • Muscle Endurance Test using Stopwatch

    4 weeks

  • Neck Disability Index

    4 weeks

Study Arms (2)

Ribs Mobilization

EXPERIMENTAL

will receive Maitland first and second Rib Mobilization with three sets of 6-8 repetitions in each session and conventional(Baseline) Physical therapy Treatment.

Other: Ribs Mobilization

Conventional Treatment

ACTIVE COMPARATOR

will only receive Baseline Physical therapy treatment

Other: Conventional treatment

Interventions

Three sets of 6-8 repetitions in each session and conventional(Baseline) Physical therapy Treatment.

Ribs Mobilization

* Hot pack for 8 min * Maitland Generalized Cervical Mobilizations (6-8 REPS,3 sets) * Isometric Strengthening Exercise

Conventional Treatment

Eligibility Criteria

Age20 Years - 45 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Neurological tests will be negative
  • Both genders having age between 20 to 45 years
  • Participants should have primary complaint of neck pain
  • Neck Disability Index (NDI) score of 20% or greater (i.e. 10 points or greater on a 0 to 50 scale)
  • a pain intensity of ≥4 on the 10-point Numerical Pain Rating Scale (NPRS)

You may not qualify if:

  • First and second rib fracture and dislocation
  • Past surgical history of cervical and thoracic region
  • Thoracic Outlet syndrome and Cervical radiculopathy
  • Congenital anomalies of spine and ribs

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Murtaza Rehabilitation center

Lahore, Punjab Province, 54600, Pakistan

Location

MeSH Terms

Conditions

Neck Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Syed Sramad Hussain Bukhari, MSOMPT

    Riphah International University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 22, 2025

First Posted

January 28, 2025

Study Start

March 1, 2025

Primary Completion

July 1, 2025

Study Completion

July 13, 2025

Last Updated

July 15, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will not share

Locations