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Clinical Trials/NCT06645132
NCT06645132
Active, Not Recruiting
N/A

Pilot Study to Understand the Feasibility of Implementing a Wearable Device Cueing System Following Bone Marrow Transplant

Medical College of Wisconsin1 site in 1 country15 target enrollmentOctober 28, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
Blood Cancer
Sponsor
Medical College of Wisconsin
Enrollment
15
Locations
1
Primary Endpoint
Pilot evaluation of intervention efficacy
Status
Active, Not Recruiting
Last Updated
last year

Overview

Brief 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.

Detailed 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.

Registry
clinicaltrials.gov
Start Date
October 28, 2024
End Date
September 2025
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Whitney Morelli

Principal Investigator

Medical College of Wisconsin

Eligibility Criteria

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 Criteria

  • Inability to complete 15 minutes walking unassisted

Outcomes

Primary Outcomes

Pilot evaluation of intervention efficacy

Time Frame: cumulative percent from day 1 through discharge from hospital, on average day 30

Efficacy will be evaluated by examining the percentage of time participants responded to the cued exercise prompts.

Patient feedback from participation in the study

Time Frame: day 10

Patient experience will be evaluated by looking at the central tendencies of the ratings from the post-participation evaluation survey.

Study Sites (1)

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