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Sharing Our Strength: A Research Study for Bone Marrow/Stem Cell Transplant Survivors

Not Applicable
Completed
Conditions
Acute Lymphocytic Leukemia
Psychological Distress
Hematological Cancers
Leukemia
Acute Leukemia
Multiple Myeloma
Interventions
Behavioral: Writing A (Experimental informative writing)
Behavioral: Writing B (Experimental noninformative writing)
Behavioral: Writing C (Control informative writing)
Behavioral: Writing D (Control noninformative writing)
Registration Number
NCT00701844
Lead Sponsor
University of North Carolina, Chapel Hill
Brief Summary

The Sharing Our Strength study is being conducted to help us understand people's experiences with hematopoietic stem cell transplantation and to test a new program designed to help people recover physically and emotionally after transplant.

Detailed Description

This is a study for survivors of hematopoietic stem cell transplantation (also known as bone marrow transplant), which is an intensive medical treatment for cancers such as leukemia, lymphoma, and multiple myeloma as well as other diseases. Because it is a physically and emotionally demanding treatment, many people report having ongoing physical and emotional difficulties after having a transplant. The Sharing Our Strength study is being conducted to help us understand people's transplant experiences and to test a new program designed to help them recover physically and emotionally after transplant. All parts of the study are completed by mail and telephone. Participants will receive compensation for their time.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
315
Inclusion Criteria
  • Be a transplant survivor who is 9 months to 3 years beyond transplant and not currently relapsed. and not currently relapsed
  • Be at least 18 years old now (and at least 16 when they had their transplant)
  • Speak English
  • Have telephone service
Read More
Exclusion Criteria
  • None
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
FACTORIAL
Arm && Interventions
GroupInterventionDescription
Experimental Writing Type 1Writing A (Experimental informative writing)-
Experimental Writing type 2Writing B (Experimental noninformative writing)-
Control writing type 1Writing C (Control informative writing)-
Control writing type 2Writing D (Control noninformative writing)-
Primary Outcome Measures
NameTimeMethod
Psychological AdjustmentAt screening, baseline and 3 months following intervention
Secondary Outcome Measures
NameTimeMethod
Quality of LifeAt screening, baseline and 3 months following intervention

Trial Locations

Locations (3)

Hackensack University Medical Center

🇺🇸

Hackensack, New Jersey, United States

University of North Carolina at Chapel Hill

🇺🇸

Chapel Hill, North Carolina, United States

Mount Sinai School of Medicine

🇺🇸

New York, New York, United States

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