Manual Therapy vs Stretching vs Routine Physical Therapy in Nonspecific Chronic Neck Pain
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
1 other identifier
interventional
102
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Mar 2021
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
March 1, 2021
CompletedFirst Submitted
Initial submission to the registry
May 30, 2021
CompletedFirst Posted
Study publicly available on registry
June 4, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 12, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
September 12, 2021
CompletedJanuary 11, 2022
January 1, 2022
7 months
May 30, 2021
January 8, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Visual Analog scale (VAS)
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
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 Outcomes (1)
Neck disability Index (NDI)
3 months
Study Arms (3)
Routine physical therapy
EXPERIMENTALPatients 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
Manual physical therapy with routine physical therapy
EXPERIMENTALPatients 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
Stretching physical therapy with routine physical therapy
EXPERIMENTALPatients 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
Interventions
Patients in this group will get every session routine physical therapy of 30 minutes 3 times per week on alternative days for 12 weeks
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
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
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ripah International University
Faisalabad, Punjab Pakistan, 3800, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Muhammad Kashif
Riphah International University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Masking Details
- The study would be double blinded as accessor and the participant of the study would be kept blind of the treatment group to which patient would be allocated. After the complete initial screening process, every recruited patient will be accessed by an independent assessor, expert will use outcome measuring tools. his will be recorded as baseline measurement assessment.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 30, 2021
First Posted
June 4, 2021
Study Start
March 1, 2021
Primary Completion
September 12, 2021
Study Completion
September 12, 2021
Last Updated
January 11, 2022
Record last verified: 2022-01
Data Sharing
- IPD Sharing
- Will not share