Dry Cupping for Low Back Pain
Trial Summary
What is the purpose of this trial?
This pilot study will investigate the effects of dry cupping the lumbar paraspinal muscles on lumbar spine on range of motion (ROM), blood flow as indicated by skin temperature, subjective pain, pressure pain threshold, perceived treatment effect and overall function in individuals experiencing Non-specific low back pain (NSLBP). The intervention will occur across three treatment sessions, scheduled approximately 48 hours apart. Both an intervention and placebo group will be used an a pre-/post- comparison will be conducted.
Will I have to stop taking my current medications?
The trial protocol does not specify if you need to stop taking your current medications. However, if you are currently receiving treatment for non-specific low back pain, you will need to have a 2-day break from that treatment before participating in the study.
What data supports the effectiveness of the treatment Dry Cupping for Low Back Pain?
The research suggests that dry cupping may not be more effective than a placebo (a treatment with no active effect) for improving outcomes in people with chronic low back pain. However, some studies indicate that the experience of social and professional support during treatment can impact how patients feel about their pain.12345
Is dry cupping safe for humans?
How does dry cupping treatment differ from other treatments for low back pain?
Dry cupping is unique because it involves placing cups on the skin to create suction, which is believed to improve blood flow and reduce pain, unlike standard treatments that often involve medication or physical therapy. It is a non-invasive method and can be applied to specific points on the body, such as acupoints, which may offer temporary relief from pain and improve sleep and disability in some patients.12589
Eligibility Criteria
This trial is for men and women aged 18-55 who have non-specific low back pain (NSLBP) but are otherwise healthy. Participants must not be receiving other treatments for NSLBP or any musculoskeletal condition, with a required 48-hour break before joining the study.Inclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive dry cupping treatment on lumbar paraspinal muscles across three sessions, approximately 48 hours apart
Follow-up
Participants are monitored for safety and effectiveness after treatment
Treatment Details
Interventions
- Dry Cupping
- Placebo Dry Cupping
Find a Clinic Near You
Who Is Running the Clinical Trial?
Lakehead University
Lead Sponsor