Frequency Specific Microcurrent for the Treatment of Diastasis Recti

Status Terminated

Clinical Trial Summary

Determine if frequency specific microcurrent therapy improves pain management of DRA by 30% or greater.

Clinical Trial Description

Females aged 18 years or older who are postpartum from a singleton gestation status post vaginal and with diastasis recti will be recruited. The aim of this study is to determine if frequency specific microcurrent therapy improves pain management of DRA by 30% or greater Improving DRA after microcurrent therapy in post-partum females may allow a faster, more effective return to activity thereby improving the return-to-duty transition and establishing personal readiness by meeting military fitness standards. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04060563
Study type	Interventional
Source	Mike O'Callaghan Military Hospital
Contact
Status	Terminated
Phase	N/A
Start date	January 1, 2020
Completion date	July 7, 2021

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See also
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