← Back to Search

Chiropractic Adjustment for Metabolic Syndrome (MET Trial)

N/A
Waitlist Available
Led By Tyson Perez, DC, PhD
Research Sponsored by Life University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Individuals who can walk unassisted for up to 10 minutes
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, an average of 1 year
Awards & highlights

MET Trial Summary

This trial looks to see if chiropractic care can help people with metabolic syndrome and assess how well the procedures/protocols work.

Who is the study for?
Adults over 18 with metabolic syndrome, able to provide consent and perform certain physical tasks like walking unassisted for 10 minutes. They should have a stable medication regimen if they're taking drugs for high blood sugar, blood pressure, triglycerides, or cholesterol. Pregnant individuals or those with certain medical conditions like rheumatoid arthritis or recent serious injuries are excluded.Check my eligibility
What is being tested?
The trial is exploring the feasibility of study procedures and potential benefits of chiropractic care on adults with metabolic syndrome. Participants will undergo chiropractic adjustments to see how it affects their condition.See study design
What are the potential side effects?
While not explicitly mentioned in the provided information, common side effects from chiropractic adjustments may include temporary discomfort in treated areas, fatigue, headache, or dizziness.

MET Trial Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I can walk by myself for 10 minutes.

MET Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, an average of 1 year
This trial's timeline: 3 weeks for screening, Varies for treatment, and through study completion, an average of 1 year for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Acceptability of treatment regimen for participants
Participant adherence rate
Participant retention rate
+2 more
Secondary outcome measures
Composite Autonomic Symptom Score (COMPASS-31)
Composite Autonomic Symptom Score COMPASS-31)
ECG de-trended fluctuation analysis
+13 more

MET Trial Design

1Treatment groups
Experimental Treatment
Group I: ChiropracticExperimental Treatment1 Intervention
Chiropractic adjustment
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Chiropractic adjustment
2013
N/A
~50

Find a Location

Who is running the clinical trial?

Life UniversityLead Sponsor
18 Previous Clinical Trials
392 Total Patients Enrolled
Tyson Perez, DC, PhDPrincipal InvestigatorLife University
1 Previous Clinical Trials
30 Total Patients Enrolled

Media Library

Chiropractic adjustment Clinical Trial Eligibility Overview. Trial Name: NCT05884437 — N/A
Metabolic Syndrome Research Study Groups: Chiropractic
Metabolic Syndrome Clinical Trial 2023: Chiropractic adjustment Highlights & Side Effects. Trial Name: NCT05884437 — N/A
Chiropractic adjustment 2023 Treatment Timeline for Medical Study. Trial Name: NCT05884437 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are new participants being accepted to take part in this research?

"Clinicaltrials.gov has registered that this trial, first introduced on June 1st 2023 and re-edited May 22nd 2023, is not currently enrolling participants. Nevertheless, there are a multitude of other 1524 ongoing studies actively searching for recruits right now."

Answered by AI

What is the projected result of this trial?

"The principal aim of this research project, evaluated over the course of one year on average, is to measure participant adherence. Additionally, EEG resting state functional connectivity (measured with a 64-channel hydronet cap), evoked latency (also measured using the same device during auditory oddball task) and amplitude (same procedure) will be recorded as secondary objectives."

Answered by AI
~0 spots leftby Jul 2024