Ignite Creation Date:
2024-10-26 @ 3:36 PM
Last Modification Date:
2024-10-26 @ 3:36 PM
Study NCT ID:
NCT06534957
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-07-30
Brief Title:
Online Mindfulness-based Stress Reduction for Patients Receiving Chemotherapy
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Online Mindfulness-based Stress Reduction Intervention for Patients With Breast Cancer Receiving Chemotherapy
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-08
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 goal of this prospective waitlist-controlled 11 randomized study is to evaluate if an online mindfulness-based stress reduction MBSR intervention reduces treatment-related stress levels among patients with breast cancer receiving chemotherapy
The main questions it aims to answer are
Does an online MBSR intervention reduce stress levels measured through the Perceived Stress Scale among participants
Does an online MBSR intervention reduce anxiety depression insomnia fatigue nausea diarrhea constipation pain and peripheral neuropathy measured through the PRO-CTCAE of the National Cancer Institute among participants
Researchers will compare the online MBSR intervention to no intervention to see if online MBSR reduces treatment-related stress
Participants will
Participate in an online MBSR intervention or no intervention for 6 weeks
Answer the study surveys at baseline 7 weeks and 11 weeks of follow-up
The main questions it aims to answer are
Does an online MBSR intervention reduce stress levels measured through the Perceived Stress Scale among participants
Does an online MBSR intervention reduce anxiety depression insomnia fatigue nausea diarrhea constipation pain and peripheral neuropathy measured through the PRO-CTCAE of the National Cancer Institute among participants
Researchers will compare the online MBSR intervention to no intervention to see if online MBSR reduces treatment-related stress
Participants will
Participate in an online MBSR intervention or no intervention for 6 weeks
Answer the study surveys at baseline 7 weeks and 11 weeks of follow-up
Detailed Description:
None
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