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NCT06156605 Clinical Trial

Looking Beyond the Immediate Effects of Lumbar Spinal Manipulation Using Pain Pressure Threshold in Asymptomatic Individuals

Pain Clinical Trial

— LumbarPPTUMary  

Official title:
Looking Beyond the Immediate Effects of Lumbar Spinal Manipulation Using Pain Pressure Threshold in Asymptomatic Individuals

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06156605
Other study ID # UMary1234
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 18, 2023
Est. completion date September 28, 2023

Study information
Verified date December 2023
Source University of Mary
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this clinical trial is to test in the effects of pain pressure threshold (PPT) looking out to 30 minutes in the lumbar spine. The main question[s] it aims to answer are: • Is there a difference between PPT from baseline, immediately after, or 30 minutes after compared to sham ultrasound control group? Participants will be exposed to sham ultrasound or sidelying lumbar manipulation with between groups and within group comparisons of PPT at the posterior superior iliac spine up to 30 minutes following the intervention.

Recruitment information / eligibility
Status Completed
Enrollment 55
Est. completion date September 28, 2023
Est. primary completion date September 28, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: - Asymptomatic individuals between the ages of 18-50 Exclusion Criteria: - Current low back pain (LBP) - A history of low back pain LBP within the last three months - Previous spinal surgery - Rheumatological condition or neurological symptoms or conditions - Recent ingestion of pain-relieving medications within the last 24 hours - A lumbar manipulation within three days prior to the exam - Exhibited any contraindications to manipulation - Positive findings during screening precautions

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Sidelying lumbar manipulation
R sided lumbar manipulation

Locations
Country Name City State
United States University of Mary Bismarck North Dakota

Sponsors (1)
Lead Sponsor Collaborator
University of Mary

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain pressure threshold PPT at the right PSIS Baseline, Immediately after, 30 minutes after
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