University of Mary
Bismarck, North Dakota, 58503, United States
NCT Number: NCT06156605
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.
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Notify Me18 year–50 year
All sexes
Interventional
Not applicable
Bismarck, North Dakota, 58503, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
R sided lumbar manipulation
Time frame: Baseline, Immediately after, 30 minutes after
PPT at the right PSIS
University of Mary
Other
Acronym: LumbarPPTUMary
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