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Not yet recruitingNCT07702617Updated Jul 22, 2026

Effects Of Vacuum Controlled Static Versus Vacuum Controlled Dynamic Dry Cupping On Pain, Range Of Motion And Disability Among Patients With Chronic Low Back Pain

An interventional study of Vacuum-Controlled Static Dry Cupping and Vacuum-Controlled Dynamic Dry Cupping in Chronic Low-back Pain (cLBP), sponsored by Lahore University of Biological and Applied Sciences. Not yet recruiting at 1 site in Pakistan. Open to participants aged 30 Years to 40 Years. Per ClinicalTrials.gov, last updated 2026-07-22.

Sponsored by Lahore University of Biological and Applied Sciences · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
48
Allocation
Randomized
Ages
30 Years to 40 Years
Sex
All
01

Study summary

This randomized controlled clinical trial aims to compare the effects of vacuum-controlled static dry cupping and vacuum-controlled dynamic dry cupping on pain intensity, lumbar range of motion, and functional disability in patients with chronic low back pain. Participants will be randomly assigned to two groups receiving either static or dynamic dry cupping along with conventional treatment. The outcomes will be assessed to determine which cupping technique is more effective in improving pain, mobility, and functional ability in individuals with chronic low back pain.

[Time Frame: Measured at baseline (pre-intervention) and after 6 weeks (post-intervention completion).

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Conditions studied

  • Chronic Low-back Pain (cLBP)
03

In context

Lead sponsor

Lahore University of Biological and Applied Sciences is the lead sponsor of 75 studies on the registry; 55 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
30 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Age 30 to 40 years. (21)
  • Both male and female genders (15)
  • Patients experiencing LBP with a score of at least 3/10 on the NPRS (22)
  • For more than three months (22).
  • Individuals whose workstations have not been ergonomically designed and who have not previously received structured ergonomic interventions related to workplace layout, task design, or load modification also involving home tasks and daily activities. (31)

Exclusion criteria

Exclusion Criteria:

  • * Subjects with lower body condition (i.e., spondylolisthesis, spinal stenosis, osteoporosis, or intervertebral disk derangement) (15)

    • Subjects with a history of cancer (15)
    • Subjects experiencing referred leg symptoms (15)
    • Subjects with any current local or systemic infections, vascular disease, including varicose veins (17)
    • History of spine surgery or spinal tumor (17).
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
48 participants (estimated)

Study arms

  • Experimental
    Static Dry Cupping

    Participants in this group will receive vacuum-controlled static dry cupping applied to the lumbar region. The cups will be placed on specific points over the lower back and kept stationary for approximately 10 minutes per session along with conventional physiotherapy management for chronic low back pain.

    Other: Vacuum-Controlled Static Dry Cupping

  • Active comparator
    Dynamic Dry Cupping

    Participants in this group will receive vacuum-controlled dynamic dry cupping applied to the lumbar region. After creating negative pressure, the cups will be gently moved over the lower back to mobilize soft tissues along with conventional physiotherapy management for chronic low back pain.

    Other: Vacuum-Controlled Dynamic Dry Cupping

Interventions

  • OtherVacuum-Controlled Static Dry Cupping

    Vacuum-controlled static dry cupping will be applied to the lumbar region of patients with chronic low back pain. Cups will be placed on the affected area and kept stationary for approximately 10 minutes to create negative pressure, aiming to improve blood circulation, reduce pain, and relieve muscle tension.

  • OtherVacuum-Controlled Dynamic Dry Cupping

    Vacuum-controlled dynamic dry cupping will be applied to the lumbar region. After creating negative pressure, the cups will be gently moved over the skin to mobilize soft tissues, enhance circulation, reduce pain, and improve lumbar mobility in patients with chronic low back pain.

06

What researchers measure

Primary outcomes

  1. Pain Intensity

    Pain intensity in patients with chronic low back pain will be assessed using the Numeric Pain Rating Scale (NPRS). The NPRS is an 11-point scale ranging from 0 to 10, where 0 indicates no pain and 10 represents the worst imaginable pain. It will be used to evaluate the effectiveness of vacuum-controlled static and dynamic dry cupping in reducing pain levels.

    Time frame: Baseline (before treatment) and after 6 weeks of intervention.

  2. Lumbar Range of Motion

    Lumbar range of motion will be measured to assess improvement in spinal mobility in patients with chronic low back pain. Lumbar movements including flexion, extension, and lateral flexion will be evaluated using a goniometer or inclinometer.

    Time frame: Baseline (before treatment) and after 6 weeks of intervention.

  3. Functional Disability

    Functional disability related to chronic low back pain will be assessed using the Oswestry Disability Index (ODI), a validated questionnaire that measures the impact of back pain on daily activities such as walking, sitting, standing, and personal care.

    Time frame: Baseline (before treatment) and after 6 weeks of intervention.

07

Study locations

1 site
  • Sehat Medical Complex
    Lahore, Punjab Province 54000, Pakistan
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07702617
Lead sponsor
Lahore University of Biological and Applied Sciences
Responsible party
Sponsor
First posted
Jul 14, 2026
Start date
Jul 1, 2026 (estimated)
Primary completion
Oct 30, 2026 (estimated)
Completion
Nov 30, 2026 (estimated)
Last update
Jul 22, 2026

Study contacts

SHOAIB WAQAS
Contact
shoaib.waqas@ubas.edu.pk
03024552109
Khizra Hamid
Contact
khizra.hamid@ubas.edu.pk
03154425879
Shoaib Waqas
study chair · Lahore University of Biological and Applied Sciences

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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