- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07595146
Meaning-Centered Psychotherapy for Addressing Existential Distress of Patient/Caregiver Dyads Following Hematopoietic Stem Cell Transplantation: Feasibility and Acceptability
May 12, 2026 updated by: Natalie S. McAndrew, PhD, RN, Mayo Clinic
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 Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
100
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Study Team
- Phone Number: 507-422-5523
- Email: rstnursingresearch@mayo.edu
Study Locations
-
-
Minnesota
-
Rochester, Minnesota, United States, 55905
- Mayo Clinic
-
Contact:
- Study Team
- Phone Number: 507-422-5523
- Email: rstnursingresearch@mayo.edu
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Meaning-Centered Psychotherapy (MCP) Dyad
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
|
Survivor and caregiver dyads will participate in a seven-session, telehealth delivered Meaning-Centered Psychotherapy for Dyads (MCP-Dyad) program post-transplant.
|
|
Active Comparator: Usual Care
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.
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Survivor and caregiver dyads will receive standard resources and consultations for hematopoietic stem cell transplantation (HSCT) care, which include a joint educational class for patients and caregivers before and after treatment.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Feasibility to accrue HSCT patient/caregiver dyads
Time Frame: Baseline
|
Percentage of eligible caregivers approached who consent and enroll within 18 months.
|
Baseline
|
|
Completion of MCP-Dyad
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%).
|
End of treatment (approximately 14 weeks)
|
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MCP-Dyad Feasibility rating from participants
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.
|
End of treatment (approximately 14 weeks)
|
|
MCP-Dyad Retention
Time Frame: End of treatment (approximately 14 weeks)
|
Percentage of patients and caregivers who complete follow-up assessments (benchmark: 75%).
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End of treatment (approximately 14 weeks)
|
|
MCP-Dyad Intervention Adherence
Time Frame: End of treatment (approximately 14 weeks)
|
Percentage of recorded sessions that are delivered per protocol (benchmark: 80%)
|
End of treatment (approximately 14 weeks)
|
|
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.
|
End of treatment (approximately 14 weeks)
|
|
Change in Intervention Appropriateness Measure (IAM) score
Time Frame: Baseline, 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.
|
Baseline, End of treatment (approximately 14 weeks)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Functional Assessment of Cancer Therapy -Bone Marrow Transplant (FACT-BMT) score
Time Frame: Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
|
The impact of MCP-Dyad on patient and caregiver health-related quality of life will be assessed using the Functional Assessment of Cancer Therapy -Bone Marrow Transplant (FACT-BMT).
The patient instrument is a multidimensional measure of quality of life in adult HSCT patients.
Each item is rated from 0 (not at all) to 4 (very much) and is an assessment of symptoms over the past 7 days.
Domains include social and family well-being, emotional well-being, functional well-being, and BMT-specific concerns.
Higher scores overall indicate better quality of life.
|
Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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Change in Life Attitude Profile-Revised (LAP-R) score
Time Frame: Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
|
The impact of MCP-Dyad on the patient and caregiver's meaning and purpose (increased meaning and purpose equivalent to less existential distress) will be measured using the 48-item Life Attitude Profile-Revised (LAP-R) instrument.
It has six domains (purpose, coherence, life control, death acceptance, existential vacuum, goal seeking) that make up two subscales, the Personal Meaning Index and Existential Transcendence.
Higher scores generally indicate a more positive attitude towards life.
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Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
|
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Change in Functional Assessment of Chronic Illness Therapy Spiritual Well-being (FACIT-Sp) Scale score
Time Frame: Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
|
The impact of MCP-Dyad on the patient's and caregiver's spiritual well-being will be measured using the Functional Assessment of Chronic Illness Therapy Spiritual Well-being (FACIT-Sp) Scale.
It has two subscales, one for faith and another for meaning/peace.
Higher scores indicate greater spiritual well-being.
|
Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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Change in Benefit Finding Scale (BFS) score
Time Frame: Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
|
The impact of MCP-Dyad on benefit finding will be measured using a slightly modified version of the Benefit Finding Scale (BFS), a 17-item measure that captures positive life challenges resulting from adversity (e.g., personal priorities, acceptance, daily activities, family, world views, relationship, purpose).
Higher scores indicate greater benefit finding.
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Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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Change in Mutuality Scale (MS) score
Time Frame: Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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The Mutuality Scale (MS) measures the positive quality of the relationship between the care recipient and the caregiver.
Grounded in the concept of mutuality (degree of love, reciprocity, shared pleasurable activities, and shared values) in the patient/caregiver relationship.
There is a four-domain structure with items rated from 0 (not at all) to 4 (a great deal) with question stems examining varies aspects of the relationship (e.g., how much do you enjoy spending time together).
Higher overall scores indicate greater mutuality.
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Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
|
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Change in Revised Dyadic Adjustment Scale (RDAS) score
Time Frame: Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
|
The Revised Dyadic Adjustment Scale (RDAS) is a self-report measure of relationship quality in couples.
It assesses dyadic consensus, dyadic satisfaction, and dyadic cohesion to give an overall index of marital quality.
The rating scale is 0 (always disagree) to 5 (always agree).
Higher overall scores indicates greater relationship satisfaction.
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Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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Change in Social Constraints Scale score
Time Frame: Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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The Social Constraints Scale measures the extent to which individuals perceive their social environment, particularly close relationships, as a limiting or discouraging their ability to express thoughts and feelings related to a stressful experience.
Items are rated from 1(never) to 4 (very often).
Higher scores are equivalent to more social constraints in the relationship.
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Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
|
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Change in Communal Coping Domains score
Time Frame: 8 weeks post-intervention
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The Communal Coping Domains instrument assesses how patients and caregivers manage health-related behavior change, particularly in the context of health threats by measuring shared perceptions, confidence, and behaviors.
There are three tailored subscales: use of communal coping (how frequently dyads use joint efforts to manage health threats), how confident the dyad is in working together to manage health, and beliefs about communal coping strategies.
Responses for the use of the communal coping domain range from 1(never) to 5 (very often), and responses for the couple efficacy and outcome efficacy range from 0 (not at all) to 10 (very much).
Higher overall scores indicate greater confidence in patient/caregiver coping strategies.
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8 weeks post-intervention
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Percentage of dyads to use plural pronouns (I versus We language)
Time Frame: Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
|
Communal coping can be objectively measured based on the amount of "we versus I" language across the intervention sessions.
Linguistic Inquiry and Word Count (LIWC-22) software is a validated way to examine the number of pronouns uttered.
Essentially, this software works by comparing each word in a text against an internal dictionary of words and then provides a percentage of total words that fall into a specific category.
We will use the recorded sessions to determine the percentage of subjects using plural pronouns.
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Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Natalie McAndrew, PhD, RN, Mayo Clinic
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
August 1, 2026
Primary Completion (Estimated)
February 28, 2028
Study Completion (Estimated)
April 30, 2028
Study Registration Dates
First Submitted
May 12, 2026
First Submitted That Met QC Criteria
May 12, 2026
First Posted (Actual)
May 19, 2026
Study Record Updates
Last Update Posted (Actual)
May 19, 2026
Last Update Submitted That Met QC Criteria
May 12, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- 26-005192
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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