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N/A Completed N=92 Randomized Supportive Care

Psychological Intervention for Caregivers of Patients Undergoing Stem Cell Transplant

Source: ClinicalTrials.gov NCT03328663 ↗
Enrolled (actual)
92
Serious AEs
0.0%
Results posted
Mar 2026
Primary outcomePrimary: Feasibility of the Intervention (Feasibility Description Below) — 36 Participants

Summary

This research study is evaluating the impact of a psychological intervention on the quality of life and mood of caregivers of patients undergoing stem cell transplant.

Outcome Measures

OutcomeResultp-value
PRIMARY
Feasibility of the Intervention (Feasibility Description Below)
36 —
SECONDARY
Compare Caregiver Quality of Life (QOL) as Measured by the Caregiver Oncology QOL (CarGOQOL) Questionnaire Between the Study Arms
81.22; 70.96 —
SECONDARY
Compare Caregiving Burden (CRA) Between the Study Arms
46.95; 55.06 —
SECONDARY
Compare Caregiver Anxiety Using Hospital Anxiety and Depression Scale (HADS) Between the Study Arms
3.62; 7.22 —
SECONDARY
Compare Caregiver Self-efficacy Using the Cancer Self-Efficacy Scale-Transplant (CASE-t) Between the Study Arms
156.20; 147.06 —
SECONDARY
Compare Perceived Coping Skills (MOCS) Between the Study Arms
36.54; 28.02 —

Eligibility Criteria

Inclusion Criteria

  • Adult caregivers (≥18 years) of patients undergoing autologous or allogeneic HCT at MGH, and they must attend the HCT consent visit with the patient.
  • A relative or a friend who either lives with the patient or has in-person contact with him or her at least twice per week and is identified as the primary caregiver for transplant.
  • Ability to speak English or able to complete questionnaires with minimum assistance of an interpreter.

Exclusion Criteria

  • Significant uncontrolled psychiatric or other co-morbid disease, which the primary oncologist believes prohibits the ability to participate in study procedures
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03328663). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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