Enhancing Resilience in Senior Community Residents

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Mass General Brigham

Status

Completed

Conditions

Quality of Life
Stress, Psychological

Treatments

Behavioral: SMART-3RP Group Intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT05438134
2021A019096

Details and patient eligibility

About

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.

Full 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 1:1 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.

Enrollment

288 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Resident of an Erickson Senior Living community
  • Currently residing in an Erickson Senior Living apartment home
  • Sufficient English language skills to participate in study procedures

Exclusion criteria

  • Unable or unwilling to provide informed consent
  • Unable or unwilling to participate in in-person group sessions

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

288 participants in 2 patient groups

SMART-3RP Group Intervention
Experimental group
Description:
Residents will participate in 9 structured weekly group sessions which incorporates stress management and relaxation training upon enrollment.
Treatment:
Behavioral: SMART-3RP Group Intervention
Waitlist Control Group Intervention
Active Comparator group
Description:
Residents will participate in 9 structured weekly group sessions which incorporates stress management and relaxation training after the final survey time point.
Treatment:
Behavioral: SMART-3RP Group Intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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