Meaning-Centered Psychotherapy for Addressing Existential Distress of Patient/Caregiver Dyads Following Hematopoietic Stem Cell Transplantation: Feasibility and Acceptability
10 agosto 2026 aggiornato da: 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.
Panoramica dello studio
Stato
Non ancora reclutamento
Condizioni
Intervento / Trattamento
Tipo di studio
Interventistico
Iscrizione (Stimato)
100
Fase
- Non applicabile
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Contatto studio
- Nome: Study Team
- Numero di telefono: 507-422-5523
- Email: rstnursingresearch@mayo.edu
Luoghi di studio
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Minnesota
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Rochester, Minnesota, Stati Uniti, 55905
- Mayo Clinic
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Contatto:
- Study Team
- Numero di telefono: 507-422-5523
- Email: rstnursingresearch@mayo.edu
-
-
Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
No
Descrizione
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
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Terapia di supporto
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: 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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Comparatore attivo: 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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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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MCP-Dyad acceptability as rated on the Acceptability of Intervention Measure (AIM)
Lasso di tempo: 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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Feasibility to accrue HSCT patient/caregiver dyads
Lasso di tempo: 2 years
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Percentage of eligible caregivers approached who consent and enroll within 24 months.
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2 years
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MCP-Dyad intervention completion
Lasso di tempo: 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 (Feasibility of Intervention Measure-FIM)
Lasso di tempo: 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
Lasso di tempo: End of treatment (approximately 14 weeks)
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Percentage of randomized dyads with both members completing follow-up assessments (benchmark: 75%).
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End of treatment (approximately 14 weeks)
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MCP-Dyad intervention fidelity and protocol delivery
Lasso di tempo: End of treatment (approximately 14 weeks)
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Percentage of audited sessions meeting intervention fidelity standards and delivered per protocol based on fidelity assessments (benchmark: ≥80%)
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End of treatment (approximately 14 weeks)
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MCP-Dyad appropriateness as rated on the Intervention Appropriateness Measure (IAM)
Lasso di tempo: 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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End of treatment (approximately 14 weeks)
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MCP-Dyad dyad-level retention outreach
Lasso di tempo: End of treatment (approximately 14 weeks)
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Percentage of missed sessions or assessments that receive outreach within 2 days (benchmark: ≥85%).
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End of treatment (approximately 14 weeks)
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Change in Benefit Finding Scale (BFS) score
Lasso di tempo: 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 Communal Coping Domains score
Lasso di tempo: 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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Change in survivor and caregiver health-related quality of life.
Lasso di tempo: 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 survivor and caregiver existential distress
Lasso di tempo: 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 survivor and caregiver spiritual well-being
Lasso di tempo: 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 survivor and caregiver mutuality (quality of relationship)
Lasso di tempo: Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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The impact of MCP-Dyad on survivor and caregiver mutuality will be measured using Mutuality Scale (MS).
The Mutuality Scale 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 dyadic adjustment (couples only)
Lasso di tempo: Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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The impact of MCP-Dyad in couples will be measured using the Revised Dyadic Adjustment Scale (RDAS).
The 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 illness-related communication
Lasso di tempo: Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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The change in illness-related communication will be measured using the Social Constraints Scale.
This 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 survivor and caregiver needs/distress
Lasso di tempo: Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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The impact of MCP-Dyad on the survivor and caregiver's needs/distress will be measured using the Cancer SupportSource Survivors: CCS-15+ and the CancerSupportSource-Caregiver: CCS-Caregiver-18+ instruments.
Survivors and caregivers will rate their level of concern from 0 (not at all) to 4 (very serious concern).
Questions for survivors focus on emotional well-being, symptom burden & impact, body image & healthy lifestyle, health care team communication, relationships & intimacy.
Questions for caregivers focus on 5 areas of concern (emotional well-being, survivor well-being, caregiving tasks, finances, and healthy lifestyle) and areas of desired support.
A total score for distress is recommended based on 18 items.
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Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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Change in survivor and caregiver psychological distress
Lasso di tempo: Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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The impact of MCP-Dyad on psychological distress will be measured using 2 anxiety and 2 depression questions from the CCS-15+ and the CCS-Caregiver-18+.
These questions have established clinical cut offs.
Scores range from 0 to 8. Survivor scores of 3 or above signify clinically significant anxiety or depression.
Caregiver anxiety scores of 4 and above, and depression scores of 3 or above, indicate clinically significant distress.
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Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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Change in Dyadic Relationship Scale score
Lasso di tempo: Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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The Dyadic Relationship Scale is a brief dyadic measure assessing positive dyadic interaction and negative dyadic strain from both caregiver and care recipient perspectives.
The caregiver version includes 11 items and the care recipient version includes 10 items, with two subscales: positive dyadic interaction and negative dyadic strain.
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Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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Change in interdependence of survivor and caregiver
Lasso di tempo: Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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The Inclusion of Other in the Self Scale is a single-item pictorial measure of perceived relationship closeness and self-other overlap.
Respondents select one of seven increasingly overlapping circle pairs to represent their relationship with a specified other person, with higher scores indicating greater perceived closeness.
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Baseline, End of treatment (approximately 14 weeks), 8 weeks post-intervention
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Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Sponsor
Investigatori
- Investigatore principale: Natalie McAndrew, PhD, RN, Mayo Clinic
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio (Stimato)
1 dicembre 2026
Completamento primario (Stimato)
28 febbraio 2028
Completamento dello studio (Stimato)
30 aprile 2028
Date di iscrizione allo studio
Primo inviato
12 maggio 2026
Primo inviato che soddisfa i criteri di controllo qualità
12 maggio 2026
Primo Inserito (Effettivo)
19 maggio 2026
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
12 agosto 2026
Ultimo aggiornamento inviato che soddisfa i criteri QC
10 agosto 2026
Ultimo verificato
1 agosto 2026
Maggiori informazioni
Termini relativi a questo studio
Altri numeri di identificazione dello studio
- 26-005192
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
NO
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
No
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
No
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .