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Clinical Trials/ISRCTN59915743
ISRCTN59915743
Completed
Not Applicable

Improvements in muscle recovery and delayed onset muscle soreness (DOMS) reduction after eccentric exercise with the BounceBack™ product: a randomised, double-blind, two-way crossover, placebo-controlled, pilot study

Mannatech, Inc (USA)0 sites10 target enrollmentOctober 9, 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Mannatech, Inc (USA)
Enrollment
10
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 9, 2008
End Date
TBD
Last Updated
11 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Mannatech, Inc (USA)

Eligibility Criteria

Inclusion Criteria

  • 1\. Both males and females, age \>\=18 and \<\=45 at screening
  • 2\. Body mass index (BMI) \>18 kg/m^2 and \<\=30 kg/m^2 at screening
  • 3\. Recreationally active but non\-resistance trained for the preceding 3 months
  • 4\. Agree to dietary modifications for the day prior to each visit
  • 5\. Subject agrees to all study visits
  • 6\. Must agree to use appropriate birth control methods during the active study

Exclusion Criteria

  • 1\. Non\-compliance during the screening phase of the study
  • 2\. Weight loss of \>10 pounds in the last 6 months
  • 3\. Pregnant or lactating
  • 4\. Currently attempting to become pregnant
  • 5\. Use of medications or supplements promoting weight gain (steroids, high\-protein supplements)
  • 6\. Daily use of acid blocking medication. Must agree to withhold acid blocking medication while on study (Includes all prescription and over the counter acid blockers including PPIs, H2RAs, and calcium carbonate \[Tums]).
  • 7\. Cigarette smoking
  • 8\. Abnormal physical examination
  • 9\. Subjects unable to understand or follow the study protocol
  • 10\. Subjects participating or participated in another clinical trial during the 1 month prior to screening

Outcomes

Primary Outcomes

Not specified

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