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A Resilience-Based Approach to Improve Long-term Quality of Life in Post-treatment Lymphoma Survivorship

Mass General Brigham logo

Mass General Brigham

Status

Not yet enrolling

Conditions

Lymphoma

Treatments

Other: Health Education Program
Other: SMART3RP-Lymphoma

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The goal of this trial is to learn if a resilience intervention can lead to improvements in lymphoma survivors' quality of life.

Full description

The Stress Management and Relaxation Response Resiliency Program for lymphoma survivors (SMART3RP-Lymphoma) was adapted by researchers at the MGH. This group program seeks to buffer stress and promote psychological resiliency and physical well-being through a variety of mind-body approaches, such as imagery, relaxation, and yoga, cognitive behavioral strategies, and positive psychology tools.

The main questions it aims to answer are:

  • Will survivors randomized to SMART3RP-Lymphoma demonstrate greater improvements in quality of life when compared to survivors randomized to a Health Education Program?
  • Will improvements in resiliency lead to improvements in quality of life?

To answer these questions, researchers will compare a resilience intervention tailored to the needs of lymphoma survivors (SMART3RP-Lymphoma) to a Health Education Program to see how they affect quality of life of lymphoma survivors.

Participants will:

  • Fill out 4 surveys across 12 months
  • Participate in 8 weekly, virtual group sessions
  • Submit hair cortisol samples

Enrollment

254 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • English or Spanish speaking adults (18+ at time of enrollment)
  • Within 2 years of completing active, curative treatment for lymphoma (includes surgery, chemotherapy, immunotherapy, radiation therapy, or other)

Exclusion criteria

  • Active psychiatric or cognitive comorbidity as determined by the site PI or treating clinician

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

254 participants in 2 patient groups

Health Education Program
Active Comparator group
Description:
Participants will participate in 8 weekly sessions. Components include: * education on the co-occurrence of mental and physical problems * goal setting for health behavior change * self-monitoring HEP is an active control condition for mind body programs and is structurally equivalent to SMART3RP
Treatment:
Other: Health Education Program
SMART3RP-Lymphoma
Experimental group
Description:
Participants will participate in 8 weekly sessions. The intervention components include: * Eliciting the relaxation response (RR), * CBT strategies to improve stress management * Positive psychology strategies to achieve growth enhancement
Treatment:
Other: SMART3RP-Lymphoma

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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