Hormonal and Bone Turnover Marker Response to an Acute Bout of Resistance or Plyometric Exercise
NCT ID: NCT00572871
Last Updated: 2016-10-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
12 participants
OBSERVATIONAL
2007-12-31
2009-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Efficacy of Plyometrics to Increase Bone Mass in Men With Osteopenia
NCT00572104
Effects of Physical Training on Bone Turnover and Quality of Life in Osteopenic Postmenopausal Women.
NCT03195517
Bone Response to Exercise in Women on Antiresorptive Medications
NCT04275011
Efficacy of Structured Exercise-Nutritional Intervention on Sarcopenia in Patients With Osteoporosis
NCT06287502
Feasibility of a Novel Resistance Exercise in Individuals With Osteoporosis
NCT05060380
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
CROSS_SECTIONAL
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Exercise after fasting
Will complete 2 resistance exercise sessions and 2 plyometric exercise sessions after a 10-hour fast
resistance exercise
single bout of resistance exercise
No exercise
Will complete a ten-hour fast but do no exercise
No exercise
Will not do any exercise
Exercise after snack
Will complete 2 resistance exercise sessions and 2 plyometric exercise sessions 2 hours following a 500 calorie nutritional supplement
plyometric exercise
single bout of plyometric exercise
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
plyometric exercise
single bout of plyometric exercise
resistance exercise
single bout of resistance exercise
No exercise
Will not do any exercise
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* No symptoms of disease
* Non-sedentary
* Age 25-65
Exclusion Criteria
* Previous or current medical condition affecting bone health, including osteoporosis.
* Cardiovascular disease
* Metallic implants affecting accuracy of bone density scan
* Current smoker
* Current participation in high-intensity jumping or resistance exercise in the last 3 months.
25 Years
65 Years
MALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Missouri-Columbia
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Pamela S Hinton, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
University of Missouri-Columbia
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
65438
Identifier Type: OTHER
Identifier Source: secondary_id
1097239
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.