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Peer Support Intervention for Caregivers of Patients Undergoing HSCT

Peer Support Intervention for Caregivers of Patients Undergoing Hematopoietic Stem Cell Transplantation: Feasibility and Preliminary Efficacy Trial

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07577674
Acronym
STEPP-Care
Enrollment
90
Registered
2026-05-11
Start date
2026-09-30
Completion date
2031-09-30
Last updated
2026-05-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hematopoietic Stem Cell Transplantation

Keywords

Caregivers, Stem Cell Transplantation

Brief summary

The main purpose of this study is to determine if a tailored peer support intervention (STEPP-Care) is feasible among caregivers of patients undergoing hematopoietic stem cell transplantation (HSCT).

Detailed description

Caregivers play a vital role in recovery following hematopoietic stem cell transplantation (HSCT). However, caregiving can contribute to psychological distress and reduced quality of life (QOL). Additionally, HSCT caregivers report low self-efficacy and social support, protective factors which would otherwise help bolster their confidence in coping with the uncertainties and challenges of HSCT. Given the challenges and unmet psychosocial needs of HSCT caregivers, peer support interventions are poised to promote caregiver coping to address caregiver distress and quality of life concerns. With limited tailored peer support interventions, for HSCT caregivers, this study aims to assess the feasibility and acceptability of a peer support intervention (STEPP-Care) and examine its preliminary effects for improving QOL, caregiver burden, and psychological well-being compared to usual care in 90 caregivers of HSCT recipients.

Interventions

BEHAVIORALSTEPP-Care

STEPP-Care is a phone-delivered six-session structured peer support intervention for caregivers of patients undergoing hematopoietic stem cell transplantation.

Sponsors

Brigham and Women's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult caregivers (≥18 years of age) of patients with hematologic malignancies who are undergoing autologous or allogeneic HSCT at Dana-Farber Cancer Institute. * Is a relative or friend who is identified by the patient to be their caregiver. * Ability to speak, read, and respond in English * Has access to a phone.

Exclusion criteria

* Caregivers with acute or unstable psychiatric conditions or other cognitive conditions that the treating oncologist believes would prohibit informed consent or ability to adhere to study procedures.

Design outcomes

Primary

MeasureTime frameDescription
Intervention Feasibilityup to 10 weeksFeasibility can be defined as \>/= 60% of STEPP-Care recipients completing 4/6 sessions
Intervention Acceptabilityup to 10 weeksAcceptability can be defined as average STEPP-Care intervention participant ratings \>20 on the Client Satisfaction Questionnaire

Contacts

CONTACTHermioni L. Amonoo, MD, MPP, MPH
hermioni_amonoo@dfci.harvard.edu617-525-7472
CONTACTJosephine Monahan, BA
jamonahan@bwh.harvard.edu
PRINCIPAL_INVESTIGATORHermioni L. Amonoo, MD, MPP, MPH

Brigham and Women's Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 12, 2026