Completed

Emotional Needs of Caregivers and Patient/Spouse Couples During Hematopoietic Stem Cell Transplantation (HSCT)

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What is being tested

Data Collection

Who is being recruted

Urogenital Diseases+41

+ Blood Protein Disorders

+ Bone Marrow Diseases

Over 21 Years
See all eligibility criteria
How is the trial designed

Interventional
Study Start: March 2002
See protocol details

Summary

Principal SponsorFred Hutchinson Cancer Center
Last updated: January 14, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: March 1, 2002

Actual date on which the first participant was enrolled.

OBJECTIVES: * Assess expression of emotion, as a function of patient presence, among spousal or other cohabiting caregivers (CG) of post-hematopoietic stem cell transplantation patients. * Assess desynchrony among subjective (self-report) and expressive indicators of emotion, as a function of patient presence, in these participants. * Correlate CG dispositional inhibition and desynchrony with physical and marital satisfaction in these participants. OUTLINE: Caregivers (CG) complete written questionnaires assessing demographics, positive and negative affect, dispositional inhibition, marital satisfaction, and physical health over 45 minutes to 1 hour on day 1. CG then engage in two oral emotional expression exercises (on the topic of caregiving and the transplant) over 2 hours on day 2. Patients are present for one oral emotional expression exercise. Participants are followed at 2 weeks and 6 months. PROJECTED ACCRUAL: A total of 60 patient/spouse couples will be accrued for this study within 18 months.

Official TitleEmotional Needs of Caregivers and Patient/Spouse Couples During Hematopoietic Stem Cell Transplantation (HSCT) 
NCT00082654
Principal SponsorFred Hutchinson Cancer Center
Last updated: January 14, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 21 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Urogenital DiseasesBlood Protein DisordersBone Marrow DiseasesBreast DiseasesBreast NeoplasmsCardiovascular DiseasesDiseaseFemale Urogenital Diseases and Pregnancy ComplicationsHematologic DiseasesHemorrhagic DisordersImmune System DiseasesImmunoproliferative DisordersLeukemiaLymphatic DiseasesLymphomaLymphoproliferative DisordersMultiple MyelomaMyelodysplastic SyndromesMyeloproliferative DisordersNeoplasmsNeoplasms by Histologic TypeNeoplasms by SiteNeoplasms, Germ Cell and EmbryonalNeoplasms, Glandular and EpithelialNeoplasms, Nerve TissueNeuroblastomaParaproteinemiasPathologic ProcessesPlasmacytomaPrecancerous ConditionsPregnancy ComplicationsPregnancy Complications, NeoplasticPreleukemiaSkin DiseasesSyndromeTrophoblastic NeoplasmsVascular DiseasesNeuroectodermal TumorsNeuroectodermal Tumors, Primitive, PeripheralNeuroectodermal Tumors, PrimitiveNeoplasms, NeuroepithelialHemostatic DisordersNeoplasms, Plasma CellMyelodysplastic-Myeloproliferative Diseases

Criteria

DISEASE CHARACTERISTICS: * In a marriage OR long-term, committed, heterosexual or homosexual, cohabiting relationship in which one member is post-hematopoietic stem cell transplantation * Patients must meet the following criteria: * At least 1 year since prior first bone marrow, stem cell, or umbilical cord blood transplantation * Allogeneic or autologous * Diagnosis of malignancy, myelodysplasia, or non-malignancy * No indication of possible or confirmed relapse * Spouse/caregiver (CG) must meet the following criteria: * Serve as the primary CG to the patient * No prior or concurrent neurologic disorder PATIENT CHARACTERISTICS: Age * 21 and over Performance status * Not specified Life expectancy * Not specified Hematopoietic * Not specified Hepatic * Not specified Renal * Not specified Other * No concurrent major psychiatric disorder * English-speaking PRIOR CONCURRENT THERAPY: Biologic therapy * See Disease Characteristics Chemotherapy * Not specified Endocrine therapy * Not specified Radiotherapy * Not specified Surgery * Not specified

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Fred Hutchinson Cancer Research Center

Seattle, United StatesSee the location
CompletedOne Study Center