Meaning-Centered Psychotherapy for Addressing Existential Distress of Patient/Caregiver Dyads Following Hematopoietic Stem Cell Transplantation: Feasibility and Acceptability
12. května 2026 aktualizováno: 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.
Přehled studie
Postavení
Zatím nenabíráme
Intervence / Léčba
Typ studie
Intervenční
Zápis (Odhadovaný)
100
Fáze
- Nelze použít
Kontakty a umístění
Tato část poskytuje kontaktní údaje pro ty, kteří studii provádějí, a informace o tom, kde se tato studie provádí.
Studijní kontakt
- Jméno: Study Team
- Telefonní číslo: 507-422-5523
- E-mail: rstnursingresearch@mayo.edu
Studijní místa
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Minnesota
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Rochester, Minnesota, Spojené státy, 55905
- Mayo Clinic
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Kontakt:
- Study Team
- Telefonní číslo: 507-422-5523
- E-mail: rstnursingresearch@mayo.edu
-
-
Kritéria účasti
Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.
Kritéria způsobilosti
Věk způsobilý ke studiu
- Dospělý
- Starší dospělý
Přijímá zdravé dobrovolníky
Ne
Popis
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
Studijní plán
Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: Randomizované
- Intervenční model: Paralelní přiřazení
- Maskování: Žádné (otevřený štítek)
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
|---|---|
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Experimentální: 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
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Survivor and caregiver dyads will participate in a seven-session, telehealth delivered Meaning-Centered Psychotherapy for Dyads (MCP-Dyad) program post-transplant.
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Aktivní komparátor: 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.
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Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Feasibility to accrue HSCT patient/caregiver dyads
Časové okno: Baseline
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Percentage of eligible caregivers approached who consent and enroll within 18 months.
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Baseline
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Completion of MCP-Dyad
Časové okno: End of treatment (approximately 14 weeks)
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Percentage of patients and caregivers in the MCP-Dyad cohort who complete at least 5 out of 7 intervention sessions (benchmark: 70%).
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End of treatment (approximately 14 weeks)
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MCP-Dyad Feasibility rating from participants
Časové okno: End of treatment (approximately 14 weeks)
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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.
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End of treatment (approximately 14 weeks)
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MCP-Dyad Retention
Časové okno: End of treatment (approximately 14 weeks)
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Percentage of patients and caregivers who complete follow-up assessments (benchmark: 75%).
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End of treatment (approximately 14 weeks)
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MCP-Dyad Intervention Adherence
Časové okno: End of treatment (approximately 14 weeks)
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Percentage of recorded sessions that are delivered per protocol (benchmark: 80%)
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End of treatment (approximately 14 weeks)
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MCP-Dyad acceptability as rated on the Acceptability of Intervention Measure (AIM)
Časové okno: End of treatment (approximately 14 weeks)
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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.
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End of treatment (approximately 14 weeks)
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Change in Intervention Appropriateness Measure (IAM) score
Časové okno: Baseline, End of treatment (approximately 14 weeks)
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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.
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Baseline, End of treatment (approximately 14 weeks)
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Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Change in Functional Assessment of Cancer Therapy -Bone Marrow Transplant (FACT-BMT) score
Časové okno: Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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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.
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Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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Change in Life Attitude Profile-Revised (LAP-R) score
Časové okno: Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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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
Časové okno: Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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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.
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Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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Change in Benefit Finding Scale (BFS) score
Časové okno: Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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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
Časové okno: 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
Časové okno: Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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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
Časové okno: 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
Časové okno: 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)
Časové okno: Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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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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Spolupracovníci a vyšetřovatelé
Zde najdete lidi a organizace zapojené do této studie.
Sponzor
Vyšetřovatelé
- Vrchní vyšetřovatel: Natalie McAndrew, PhD, RN, Mayo Clinic
Termíny studijních záznamů
Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.
Hlavní termíny studia
Začátek studia (Odhadovaný)
1. srpna 2026
Primární dokončení (Odhadovaný)
28. února 2028
Dokončení studie (Odhadovaný)
30. dubna 2028
Termíny zápisu do studia
První předloženo
12. května 2026
První předloženo, které splnilo kritéria kontroly kvality
12. května 2026
První zveřejněno (Aktuální)
19. května 2026
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
19. května 2026
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
12. května 2026
Naposledy ověřeno
1. května 2026
Více informací
Termíny související s touto studií
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