Evaluation of a Stress Management Tool

Overview

About this study

The purpose of this study it so gather preliminary data regarding the impact a relaxation device has on stress level.

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. Please contact the study team to discuss whether or not you are eligible to participate in a study.

Inclusion Criteria:  

  • Adult, English speaking
  • Able to recline in lounge for at least 30 minutes
  • Able to participate in outcome measures (e.g., questionnaires and heart rate monitor chest strap)
  • Average stress level over past month is moderate-high (4 or higher on scale of 0 to 10)

Exclusion Criteria:

  • Implanted medical devices (e.g. Pacemaker, AICD, SC stimulator)
  • External medical devices that cannot be disconnected for 1 hour
  • Inability to recline for 30 minutes
  • Those who are pregnant

 

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

Rochester, Minn.

Mayo Clinic principal investigator

Jennifer Lee

Closed for enrollment

Contact information:

Laura Peterson NBC-HWC

(507)293-2933

rsthlpresearch@mayo.edu

More information

Publications

Publications are currently not available

Study Results Summary

Not yet available

Supplemental Study Information

Not yet available

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CLS-20309322

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