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The PRISM Intervention for Adolescents and Young Adults Receiving Hematopoietic Cell Transplantation

Seattle Children's Healthcare System logo

Seattle Children's Healthcare System

Status

Completed

Conditions

Adherence, Medication
Quality of Life
Coping Skills
Depression
Cancer
Anxiety
Adolescent Behavior
Bone Marrow Neoplasms

Treatments

Behavioral: PRISM (Promoting Resilience in Stress Management)

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT03640325
STUDY00001077 (SC-N126)
R01CA225629 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

Multisite Randomized Controlled Trial (RCT) testing the efficacy of the Promoting Resilience in Stress Management (PRISM) intervention among Adolescents and Young Adults receiving hematopoietic cell transplantation for hematology malignancy.

Full description

The experience of hematopoietic cell transplantation (HCT) for malignancy or cancer predisposition among Adolescents and Young Adults (AYAs) is particularly difficult because age-related developmental challenges of identity, relationships, and vocation may add to the burden of cancer. Compared to other age-groups, AYAs have poorer psychosocial outcomes including increased anxiety and depression and poorer adherence to oral immunosuppressive medications. These outcomes may, in turn, predispose AYAs to disease-related morbidity and mortality such as graft-versus-host disease (GVHD) and/or cancer-relapse. A potential barrier to improving these experiences may be that AYAs have few opportunities to develop the personal resources needed to handle adversity. We have previously developed the "Promoting Resilience in Stress Management" (PRISM) intervention for AYAs with serious illness. This manualized, brief intervention is delivered in 4, 30-60 minute, one-on-one sessions, followed by a Parent/ Caregiver/ Spouse/ significant other inclusive meeting. It targets skills in stress-management and mindfulness, goal-setting, positive reframing, and meaning-making. All of these skills are associated with improved patient well-being in other populations, and preliminary findings from a recently closed phase II randomized controlled trial among AYAs with newly diagnosed cancer suggest PRISM is associated with improved health-related quality of life. This study will build on our prior experience and fill a critical knowledge gap regarding PRISM's impact among AYAs receiving HCT. Thus, we will conduct a multi-site randomized controlled trial with the primary trial outcome of patient-reported symptoms of anxiety and depression. Secondary and exploratory outcomes will include the cost-effectiveness of the intervention in this population, the impact of the intervention on parent well-being, and patient adherence to oral graft-versus-host-disease medications. We hypothesize that AYAs who receive PRISM will report fewer mixed affective symptoms, while their parents report improved quality of life and psychological distress. We also anticipate the intervention will positively impact adherence and be cost-effective. In sum, this study offers an opportunity to expand the body of knowledge regarding methodologically rigorous and evidence-based psychosocial interventions and standards of care for AYAs with hematologic malignancies. Ultimately, this research has the potential to reduce the burden of cancer in these vulnerable populations.

Enrollment

143 patients

Sex

All

Ages

12 to 24 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria for adolescent/young adult (AYA) patient:

  • Patient aged 12-24 years
  • Receiving hematopoietic cell transplantation (HCT) for malignancy or cancer predisposition syndrome
  • Within 4 weeks of HCT "day zero"
  • Able to speak English
  • Able to read English or Spanish
  • Cognitively able to participate in interviews

Exclusion Criteria for AYA patient:

  • Patient refusal
  • Cognitively or physically unable to participate in interviews
  • Unable to speak English
  • Unable to read English or Spanish

For enrolled caregivers of AYA patient (no age limit):

Inclusion criteria:

  • AYA Child of caregiver agreed to participate
  • One caregiver per patient-caregiver dyad
  • Parent/guardian cognitively and physically able to participate
  • Parent/guardian is able to speak/read English or Spanish

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

143 participants in 3 patient groups

PRISM (Promoting Resilience in Stress Management)
Experimental group
Description:
Resilience Skills Training
Treatment:
Behavioral: PRISM (Promoting Resilience in Stress Management)
Usual Care
No Intervention group
Description:
Usual psychosocial care (control arm, no intervention)
Caregivers
No Intervention group
Description:
Caregivers of participants, no intervention

Trial documents
1

Trial contacts and locations

5

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Data sourced from clinicaltrials.gov

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