Understanding the Implementation of Cued Exercise Using Wearable Devices and a Custom Smartphone Application Following Bone Marrow Transplant.

Last updated: February 13, 2025
Sponsor: Medical College of Wisconsin
Overall Status: Active - Not Recruiting

Phase

N/A

Condition

Hematologic Neoplasms

Blood Cancer

Treatment

exercise intervention

Clinical Study ID

NCT06645132
PRO00051086
  • Ages > 18
  • All Genders

Study Summary

The purpose of this study is to pilot test the feasibility of providing patients diagnosed with a hematologic malignancy, undergoing an allogeneic bone marrow transplant, a wearable device and smartphone app (similar to a Fitbit), that would send personalized reminders to move during their post-transplant inpatient hospital stay to promote physical recovery and well-being.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • At least 18 years of age

  • Diagnosed with hematologic malignancy

  • Scheduled to receive an alloBMT

  • Physician consent to participate in the study

Exclusion

Exclusion Criteria:

• Inability to complete 15 minutes walking unassisted

Study Design

Total Participants: 15
Treatment Group(s): 1
Primary Treatment: exercise intervention
Phase:
Study Start date:
October 28, 2024
Estimated Completion Date:
September 30, 2025

Study Description

Enrolled patients who have been diagnosed with a hematologic malignancy and are scheduled to undergo an allogeneic bone marrow transplant will use a custom-designed wearable device and smartphone application as a behavioral intervention to cue exercise. Participants will be asked to wear the wearable device for the duration of their post-transplant inpatient hospital stay.

Aim 1. To examine the potential efficacy of the wearable device + smartphone application to prompt alloBMT patients to move.

Aim 2. To receive participant feedback on their experience participating in the study.

Connect with a study center

  • Froedtert Hospital

    Milwaukee, Wisconsin 53226
    United States

    Site Not Available

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