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Using a Small Wearable Device to Track Orientation and Activity in Pregnant Patients

Overview

About this study

The primary goal of this study is to evaluate the overall user experience of the Pregnancy Coach and ensure that it is well tolerated and used properly before moving to a larger randomized efficacy trial.

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:

  • Pregnant women between 10 to 30 weeks gestation

Exclusion Criteria: 

  • Patients with vaginal bleeding
  • severe thrombocytopenia (platelet count < 100,000/mm3)
  • oxygen saturations < 90%
  • pulmonary edema,
  • maternal intellectual disability

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

Rochester, Minn.

Mayo Clinic principal investigator

Margaret Dow, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available

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CLS-20272709

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