Ignite Creation Date:
2024-10-26 @ 3:43 PM
Last Modification Date:
2024-10-26 @ 3:43 PM
Study NCT ID:
NCT06645132
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-10-14
Brief Title:
Understanding the Implementation of Cued Exercise Using Wearable Devices and a Custom Smartphone Application Following Bone Marrow Transplant
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Pilot Study to Understand the Feasibility of Implementing a Wearable Device Cueing System Following Bone Marrow Transplant
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
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
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
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None