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A Study Of Combining Vibrotactile Coordinated Reset Fingertip Stimulation With Resistance Training In Individuals With Parkinson’s Disease.

Overview

About this study

The purpose of this study is to examine the impact of combining vibrotactile vCR to a 12-week resistance training program on parameters of clinical and functional outcomes.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:     

  • Diagnosed Parkinson’s Disease, confirmed by a neurologist.

 

Exclusion Criteria:   

  • Any additional diagnosed neurological disease, cardiovascular disease, or orthopedic issues that preclude safe participation in fingertip stimulation or resistance training.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 05/15/2025. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Eau Claire, Wis.

Mayo Clinic principal investigator

Leonardo Fugoso JR, M.D.

Contact us for the latest status

Contact information:

Leonardo Fugoso

7158381900

FugosoJr.Leonardo@mayo.edu

More information

Publications

Publications are currently not available

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CLS-20598477

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