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Not Applicable

Resistance training for Exercise Intervention

N/A
Waitlist Available
Led By Jaapna Dhillon, PhD
Research Sponsored by University of Missouri-Columbia
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
BMI: 28-40 kg/m2
Consistent diet patterns
Timeline
Screening 3 weeks
Treatment Varies
Follow Up change over 6 weeks
Awards & highlights

Study Summary

This trial will study the effects of resistance training on gut health and metabolism in obese adults.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change over 6 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and change over 6 weeks for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change in stool microbiome composition
Change in stool microbiome diversity
Secondary outcome measures
24hr appetite ratings
Change in Body mass
Change in blood pressure
+10 more
Other outcome measures
Food environment perceptions

Trial Design

2Treatment groups
Experimental Treatment
Group I: Resistance trainingExperimental Treatment1 Intervention
Participants will undergo 6 weeks of supervised resistance training
Group II: Conventional physical activity guidelinesExperimental Treatment1 Intervention
Participants are given recommendations on physical activity guidelines
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Resistance training
2008
Completed Phase 3
~1010

Find a Location

Who is running the clinical trial?

University of Missouri-ColumbiaLead Sponsor
360 Previous Clinical Trials
627,983 Total Patients Enrolled
Jaapna Dhillon, PhDPrincipal InvestigatorUniversity of Missouri-Columbia
2 Previous Clinical Trials
180 Total Patients Enrolled

Frequently Asked Questions

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

What are the key aims of this experimental research?

"The main focus of this 6-week trial is to observe changes in stool microbiome composition. Secondary objectives include monitoring levels of short chain fatty acids (acetate, propionate, and butyrate), fasting glucose values, as well as fat free mass body composition."

Answered by AI

What criteria dictate a person's eligibility for this trial?

"To qualify for this medical trial, applicants must be within the 18-35 age range and have a history of physical activity. Approximately 30 participants are needed to complete the study."

Answered by AI

Does this investigation admit participants of less than 25 years old?

"This medical study is seeking volunteers aged between 18 and 35."

Answered by AI

Are there any openings for participants in this experiment?

"Affirmative. Online data hosted on clinicaltrials.gov states that this experiment is currently looking to enrol 30 subjects at one location, with the initial posting date of May 19th 2021 and most recent update occurring September 16th 2021."

Answered by AI

What is the maximum number of enrollees for this trial?

"Affirmative. Records on clinicaltrials.gov show that this medical trial is actively enrolling participants, having been posted initially on May 19th 2021 and most recently updated September 16th 2021. 30 patients are sought from a single location for the study."

Answered by AI
~9 spots leftby Mar 2025