Manual Therapy vs Stretching vs Routine Physical Therapy in Nonspecific Chronic Neck Pain

January 8, 2022 updated by: Riphah International University

Effects of Manual Therapy Versus Stretching Versus Routine Physical Therapy on Pain, ROM, and Functional Disability in Restaurant Chef Workers With Nonspecific Chronic Neck Pain: A Randomised Controlled Trial

The aim of this study is to analyze the effect of Mulligan technique vs stretching techniques and vs routine physical therapy on pain ,range of motion(ROM) and functional disability among restaurant chefs with non-specific chronic pain.

Study Overview

Detailed Description

Neck pain (NP) is one of the basic musculoskeletal issues. Neck pain can be due to stress about the musculoskeletal framework because of postural problems and may be related with different causes, such as: - Intervertebral disc herniation, -nerve compression -fracture.

Nonspecific neck pain is a pain located in the lateral and posterior neck that does not show pathognomonic signs and symptoms. When the duration of symptoms is greater than 12 weeks of evolution, it acquires the value of chronicity, being denominated non-specific chronic neck pain (NCNP). It is a common disorder, which generates a great impact and socio-economic cost .

In this study we evaluate the comparison of manual physical therapy vs routine physical therapy vs stretching physical therapy effects among restaurants chefs having non-specific chronic pain.

Study Type

Interventional

Enrollment (Actual)

102

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Punjab Pakistan
      • Faisalabad, Punjab Pakistan, Pakistan, 3800
        • Ripah International University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 60 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Neck pain for atleast 3 months having no :

    • Neurological Problem
    • Rheumatological Problem
    • Patient had taken any analgesic medication for neck pain for last 3 months.
    • Non specific neck pain
    • Age 18-60 years

Exclusion Criteria:

  • Neck pain due to,

    • Tumors
    • Ankylosings Spondylitis
    • Fracture
    • Dislocation
    • Presence of cord compression
    • Vertebrobasilar artery insufficiency
    • Osteoprosis OR Osteopenia
    • Long term use of anticoagulant or corticosteroid drugs
    • Pain due to any congenital deformity, inflammation or any infection
    • Carcinoma

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Routine physical therapy

Patients in this group will get every session of 30 min 3 times per week on alternative days for 12 weeks

  1. TENS and hot pack for 15 minutes
  2. Ultra sound for 5 minutes
  3. ROM exercises repeats 5 times for 10 minutes
Patients in this group will get every session routine physical therapy of 30 minutes 3 times per week on alternative days for 12 weeks
Other Names:
  • Rehabilitation following Routine physical therapy
Experimental: Manual physical therapy with routine physical therapy

Patients in group B will get every session 30 minutes 3 times per week on alternative days

  1. TENS and hot pack for 15 minutes
  2. Ultra sound for 5 minutes
  3. Mulligan technique (NAGS and SNAGS) will repeats 5 times for 10 minutes
Patients in this group will get every session Manual physical therapy with routine physical therapy of 40 to 45 minutes 3 times per week on alternative days for 12 weeks
Other Names:
  • Rehabilitation following Manual physical therapy with routine physical therapy
Experimental: Stretching physical therapy with routine physical therapy

Patients in this group will get every session 30 minutes 3 times per week on alternative days

  1. TENS and hot pack for 15 minutes
  2. Ultra sound for 5 minutes
  3. Stretching exercises repeats 5 times for 10 minutes
Patients in this group will get every session of Stretching physical therapy with routine physical therapy of 40 to 45 minutes 3 times per week on alternative days for 12 weeks
Other Names:
  • Rehabilitation following Stretching physical therapy with routine physical therapy

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Visual Analog scale (VAS)
Time Frame: 3 months

Visual Analogue Scale is a measurement instrument that tries to measure a characteristic or attitude that is believed to range across a continuum of values and cannot easily be directly measured. It is often used in epidemiologic and clinical research to measure the intensity or frequency of various symptoms.

The visual analog scale (VAS) is a validated, subjective measure for acute and chronic pain. Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum between "no pain" and "worst pain

3 months
Bubble inclinometer
Time Frame: 3 months
Baseline's Bubble Inclinometer is a simple to use device for measuring range of motion in patients. The inclinometer can be used to measure range of motion in the neck, the hip, the elbow, the knee, the shoulder, the spine, the ankle, the wrist, and the MCP joint
3 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Neck disability Index (NDI)
Time Frame: 3 months
This questionnaire has been designed to give us information as to how your neck pain has affected your ability to manage in everyday life.The NDI can be scored as a raw score or doubled and expressed as a percent. Each section is scored on a 0 to 5 rating scale, in which zero means 'No pain' and 5 means 'Worst imaginable pain'. Points summed to a total score.
3 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 1, 2021

Primary Completion (Actual)

September 12, 2021

Study Completion (Actual)

September 12, 2021

Study Registration Dates

First Submitted

May 30, 2021

First Submitted That Met QC Criteria

May 30, 2021

First Posted (Actual)

June 4, 2021

Study Record Updates

Last Update Posted (Actual)

January 11, 2022

Last Update Submitted That Met QC Criteria

January 8, 2022

Last Verified

January 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • RCRAHS/FSD/REC/0260

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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