Completed

Study of the Emotional Needs of Caregivers of Stem Cell Transplantation Patients

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What is being tested

psychosocial assessment and care

Procedure
Who is being recruted

Breast Cancer
+9

+ Chronic Myeloproliferative Disorders
+ Gestational Trophoblastic Tumor
Over 21 Years
How is the trial designed

Other Study

Interventional
Study Start: March 2002

Summary

Principal SponsorFred Hutchinson Cancer Center
Last updated: September 21, 2010
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Study start date: March 1, 2002Actual date on which the first participant was enrolled.

RATIONALE: Understanding the emotional needs of spouses or others who are living with and caring for patients who have undergone stem cell transplantation may help improve the quality of life of both the caregivers and the patients. PURPOSE: This clinical trial is studying the emotional needs of caregivers of patients who have undergone stem cell transplant. 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) 
Principal SponsorFred Hutchinson Cancer Center
Last updated: September 21, 2010
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.
Design Details

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria
Any sexBiological sex of participants that are eligible to enroll.
Over 21 YearsRange of ages for which participants are eligible to join.
Healthy volunteers not allowedIf individuals who are healthy and do not have the condition being studied can participate.
Conditions
Pathology
Breast Cancer
Chronic Myeloproliferative Disorders
Gestational Trophoblastic Tumor
Leukemia
Lymphoma
Multiple Myeloma and Plasma Cell Neoplasm
Myelodysplastic Syndromes
Myelodysplastic/Myeloproliferative Diseases
Neuroblastoma
Ovarian Cancer
Psychosocial Effects of Cancer and Its Treatment
Testicular Germ Cell Tumor
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 CenterSeattle, United StatesSee the location

CompletedOne Study Center