Instrument Assisted Soft Tissue Mobilization Versus Dry Cupping On Chronic Mechanical Neck Pain
1 other identifier
interventional
45
1 country
1
Brief Summary
Which is more effective Instrument assisted soft tissue mobilization or Dry cupping on pain intensity, cervical range of motion and functional status in patients with chronic mechanical neck pain?
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 Apr 2024
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
April 23, 2024
CompletedFirst Submitted
Initial submission to the registry
May 25, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 30, 2025
CompletedFirst Posted
Study publicly available on registry
June 5, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
June 10, 2025
CompletedSeptember 25, 2025
September 1, 2025
1.1 years
May 25, 2025
September 24, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Pain intensity
Visual analogue scale will assess pain intensity.The visual analog scale (VAS) is a validated, subjective measure for acute and chronic pain. Scores are based on self-reported measures of symptoms that are recorded with a single handwritten mark placed at one point along the length of a 10-cm line that represents a continuum between the two ends of the scale- "no pain" on the left end (0 cm) of the scale and the "worst pain" on the right end of the scale (10 cm).
up to four weeks
Secondary Outcomes (1)
Cervical Range of motion
up to four weeks
Other Outcomes (1)
neck disability
up to four weeks
Study Arms (3)
intrumented assissted soft tissue mobilization
EXPERIMENTALtwenty patients Will receive Instrument assisted soft tissue mobilization and Conventional therapy (isometric exercises, stretching, posture correction exercises and cold pack) for 3 sessions per week for 4 weeks
dry cupping
EXPERIMENTALtwenty patients Will receive Dry cupping and conventional therapy (isometric exercises, stretching, posture correction exercises and cold pack) for 3 sessions per week for 4 weeks.
conventional therapy
ACTIVE COMPARATORtwenty patients will be treated with isometric exercises, stretching, posture correction exercises and cold pack) for 3 sessions per week for 4 weeks.
Interventions
for application of IASTM. the patient will sit on chair in comfortable position, apply lubricant material on treated area (trapezius muscle). Apply IASTM in 30-60 angle for 40 to 120 sec until hyperemia occur for each side+ conventional therapy
the dry cupping will be aplied by using plastic cups that are placed over localized areas of skin. A vacuum suction is achieved with a manual handheld pump device to create a negative pressure, drawing localized skin and soft tissue structures into the cup+ conventional therapy
the patients will receive Isometric strengthening exercises for cervical Extensors, Flexors, bilateral side Flexors and Rotators (resistance was about 50% of the patient's maximum strength, hold for 10 seconds, for 10 repetitions.Stretching of the upper fibers of trapezius (stretching was held for 30 seconds and repeated 3 times). postural correction exercises in the form of ; 1) Chin tucks exercise is quick and easy to do and it helps strengthening upper thoracic extensors, the muscles that align head over shoulders.2)Corner stretch: provides a deep stretch of the chest and shoulders, which can help maintain good posture.
Eligibility Criteria
You may qualify if:
- patients with chronic mechanical neck pain in the past 3 months.
- Age range from 18 to 35 years old.
- Patients will be from both sexes.
- Body mass index from 18.5 to 24.9 kg/m2.
- Subjects suffer from chronic mechanical neck pain.
You may not qualify if:
- Serious injury.
- Tumor.
- Infection.
- Spinal fractures.
- Recent cervical surgery.
- Cervical radiculopathy.
- Skin disease, allergy, hypersensitivity, any malignant or benign tumors.
- Unhealed scars or wounds.
- Pregnancy.
- Known psychiatric condition under treatment or medication.
- Any orthopedic and Neurological condition as cervical PIVD, spondylolisthesis.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Study Sites (1)
Cairo university
Cairo, Egypt
Related Publications (1)
Binder AI. Neck pain. BMJ Clin Evid. 2008 Aug 4;2008:1103.
PMID: 19445809RESULT
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Sahar Abdullah, Phd
Cairo University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Bachelor of physiotherapy
Study Record Dates
First Submitted
May 25, 2025
First Posted
June 5, 2025
Study Start
April 23, 2024
Primary Completion
May 30, 2025
Study Completion
June 10, 2025
Last Updated
September 25, 2025
Record last verified: 2025-09
Data Sharing
- IPD Sharing
- Will not share