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Clinical Trials/NCT07595146
NCT07595146Not yet recruitingNot Applicable

Meaning-Centered Psychotherapy for Addressing Existential Distress of Patient/Caregiver Dyads Following Hematopoietic Stem Cell Transplantation: Feasibility and Acceptability

Mayo Clinic1 site in 1 country100 target enrollmentStarted: December 1, 2026Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
100
Locations
1
Primary Endpoint
Feasibility to accrue HSCT patient/caregiver dyads

Study Overview

Brief Summary

The purpose of this study is to learn whether Meaning-Centered Psychotherapy (MCP-Dyad) is practical, acceptable, and helpful to survivors and caregivers during recovery after stem cell transplant. MCP-Dyad is a meaning-focused support program. It is designed to help people stay connected to meaning, cope with difficult experiences, and communicate as a pair during recovery.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Eligible patients and their caregivers must be adults (≥18 years)
  • •Patient must have undergone HSCT for a malignant blood cancer condition
  • •Caregiver must be the main support person (e.g., signed caregiving contract) for the HSCT patient
  • •Both the patient and their caregiver must be willing to participate in the study (dyads only)
  • •Be able to read, write, and speak in English
  • •Have access to a smartphone, computer, or tablet necessary for study participation and assessments. If a patient/caregiver dyad is interested in participating but does not have such a device, we will provide a Tracfone with smartphone capabilities for each member of the dyad

Exclusion Criteria

  • •Patients undergoing HSCT for nonmalignant conditions
  • •Patients and caregivers with severe cognitive or psychiatric impairment that may affect informed consent/participation
  • •Prisoners, pregnant women, and institutionalized persons
  • •Patients with severe cognitive or psychiatric impairment that would affect informed consent or participation

Arms & Interventions

Meaning-Centered Psychotherapy (MCP) Dyad

Experimental

The MCP-Dyad arm participants will meet with an MCP-Dyad interventionist to engage in didactic content, reflection, and discussion to teach participants how to apply four sources of meaning to their lives

Intervention: Meaning-Centered Psychotherapy (Behavioral)

Usual Care

Active Comparator

The standard of care arm will receive standard resources and consultations for HSCT care, which include a joint educational class for patients and caregivers before and after treatment.

Intervention: Usual Care (Behavioral)

Outcomes

Primary Outcomes

Feasibility to accrue HSCT patient/caregiver dyads

Time Frame: 2 years

Percentage of eligible caregivers approached who consent and enroll within 24 months.

MCP-Dyad intervention completion

Time Frame: End of treatment (approximately 14 weeks)

Percentage of patients and caregivers in the MCP-Dyad cohort who complete at least 5 out of 7 intervention sessions (benchmark: 70%).

MCP-Dyad Feasibility rating from participants (Feasibility of Intervention Measure-FIM)

Time Frame: End of treatment (approximately 14 weeks)

Percentage of patients and caregivers who rate MCP-Dyad as 4/5 or higher on the Feasibility of Intervention Measure (FIM) 4-item questionnaire (benchmark: 70%). Higher scores signify greater agreement with intervention feasibility.

MCP-Dyad retention

Time Frame: End of treatment (approximately 14 weeks)

Percentage of randomized dyads with both members completing follow-up assessments (benchmark: 75%).

MCP-Dyad intervention fidelity and protocol delivery

Time Frame: End of treatment (approximately 14 weeks)

Percentage of audited sessions meeting intervention fidelity standards and delivered per protocol based on fidelity assessments (benchmark: ≥80%)

MCP-Dyad appropriateness as rated on the Intervention Appropriateness Measure (IAM)

Time Frame: End of treatment (approximately 14 weeks)

Percentage of patients and caregivers who rate the intervention as 4/5 or higher on the 4-item Intervention Appropriateness Measure (IAM) questionnaire (benchmark: 70%). Higher scores signify greater agreement with intervention appropriateness.

MCP-Dyad dyad-level retention outreach

Time Frame: End of treatment (approximately 14 weeks)

Percentage of missed sessions or assessments that receive outreach within 2 days (benchmark: ≥85%).

MCP-Dyad acceptability as rated on the Acceptability of Intervention Measure (AIM)

Time Frame: End of treatment (approximately 14 weeks)

Percentage of patients and caregivers who rate the intervention as 4/5 or higher on the 4-item Acceptability of Intervention Measure (AIM) questionnaire (benchmark: 70%). Higher scores signify greater agreement with intervention acceptability.

Secondary Outcomes

  • Change in survivor and caregiver health-related quality of life.(Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention)
  • Change in interdependence of survivor and caregiver(Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention)
  • Change in survivor and caregiver existential distress(Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention)
  • Change in survivor and caregiver spiritual well-being(Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention)
  • Change in survivor and caregiver mutuality (quality of relationship)(Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention)
  • Change in dyadic adjustment (couples only)(Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention)
  • Change in illness-related communication(Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention)
  • Change in survivor and caregiver needs/distress(Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention)
  • Change in survivor and caregiver psychological distress(Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention)
  • Change in Dyadic Relationship Scale score(Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention)
  • Change in Benefit Finding Scale (BFS) score(Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention)
  • Change in Communal Coping Domains score(8 weeks post-intervention)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Natalie S. McAndrew, PhD, RN

Principal Investigator

Mayo Clinic

Study Sites (1)

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