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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00701844
Enrollment
315
Registered
2008-06-19
Start date
2007-07-31
Completion date
2011-09-30
Last updated
2017-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Leukemia, Acute Lymphocytic Leukemia, Hematological Cancers, Leukemia, Multiple Myeloma, Psychological Distress

Keywords

Aplastic Anemia, Lymphatic Diseases, Leukemia, Leukemia, Lymphoid, Immunoproliferative Disorders, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Anemia, Quality of Life, Lymphoproliferative Disorders, Lymphoma, Multiple Myeloma

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.

Interventions

BEHAVIORALWriting A (Experimental informative writing)

Experimental informative writing

BEHAVIORALWriting B (Experimental noninformative writing)

Experimental noninformative writing

BEHAVIORALWriting C (Control informative writing)

Control informative writing

BEHAVIORALWriting D (Control noninformative writing)

Control noninformative writing

Sponsors

American Cancer Society, Inc.
CollaboratorOTHER
University of North Carolina, Chapel Hill
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frame
Psychological AdjustmentAt screening, baseline and 3 months following intervention

Secondary

MeasureTime frame
Quality of LifeAt screening, baseline and 3 months following intervention

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026