Viewing Study NCT05438134



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Last Modification Date: 2024-10-26 @ 2:36 PM
Study NCT ID: NCT05438134
Status: COMPLETED
Last Update Posted: 2023-11-07
First Post: 2022-06-24

Brief Title: Enhancing Resilience in Senior Community Residents
Sponsor: Massachusetts General Hospital
Organization: Massachusetts General Hospital

Study Overview

Official Title: Enhancing Resilience in Senior Living Community Residents A Randomized Controlled Trial
Status: COMPLETED
Status Verified Date: 2023-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This randomized waitlist-controlled trial tests the efficacy of the Stress Management and Resiliency Training Relaxation Response Resiliency Program SMART-3RP a mind-body intervention to enhance resilience and flourishing among residents in continuing care retirement communities The investigators hypothesize that participants in the SMART-3RP group will report greater increases in resilience and flourishing relative to participants in the control group
Detailed Description: This randomized control trial tests the efficacy of the Stress Management and Resiliency Training Relaxation Response Resiliency Program SMART-3RP to improve resilience and flourishing among older adults residing in continuing care retirement communities relative to a wait-list control group At enrollment participants will be randomly assigned to the intervention group or the control group using computer generated 11 blocked randomization stratified by community site The intervention group will receive the SMART-3RP program immediately upon enrollment the wait-list control group will be invited to receive the SMART-3RP program after the final survey time point An estimate of 360 participants will be recruited from up to nine geographically diverse Erickson Senior Living communities

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None