Characterizing Adverse Events Reported Immediately After Osteopathic Manipulative Treatment.
Brian F Degenhardt, Jane C Johnson, William J Brooks...
https://pubmed.ncbi.nlm.nih.gov/29480914Actively Recruiting
Led by Burrell College of Osteopathic Medicine · Updated on 2025-01-09
32
Participants Needed
1
Research Sites
48 weeks
Total Duration
This research aims to determine whether osteopathic manipulative treatment (OMT) can help adults recover their sense of smell after losing it due to COVID-19 infection. Loss of smell is a common symptom of COVID-19 that affects quality of life and safety. The study will also explore how long any improvement in olfactory function lasts. Participants must be adults who tested positive for COVID-19 and currently have some loss of smell. Participants will be randomly assigned to receive either OMT or a sham treatment. The OMT involves occipitoatlantal decompression with specific pressure for 2 minutes and treatment of nasal Chapman points, both performed while lying down. The sham treatment consists of the investigator gently resting their hands on the participant's neck for 5 minutes. Olfactory testing using the "Sniffin' Sticks" method will be done before and after treatment, with follow-up tests daily for up to 10 days to assess changes in smell. Throughout the study, participants will undergo repeated smell tests and evaluations to monitor recovery. The primary outcome is the ability to regain the sense of smell from enrollment until two weeks after treatment. Safety monitoring includes screening for factors that might interfere with treatment or increase risks. The total participation involves initial assessment, treatment, and up to 10 days of follow-up testing to observe lasting effects or natural recovery of smell.
CONDITIONS
Investigating the Efficacy of OMT to Recover Olfactory Perception After COVID-19
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Total: 1 location
1
Burrell College of Osteopathic Medicine
Las Cruces, New Mexico, United States, 88001
Actively Recruiting
T
Thomas P Eiting, Ph.D
A
Adrienne Kania, D.O.
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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