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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00701844
Other study ID # GCO #06-0391 (2)
Secondary ID RSGPB-07-285-01-
Status Completed
Phase N/A
First received June 4, 2008
Last updated November 14, 2017
Start date July 2007
Est. completion date September 2011

Study information

Verified date May 2013
Source University of North Carolina, Chapel Hill
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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 information / eligibility

Status Completed
Enrollment 315
Est. completion date September 2011
Est. primary completion date September 2011
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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:

Study Design


Intervention

Behavioral:
Writing A (Experimental informative writing)
Experimental informative writing
Writing B (Experimental noninformative writing)
Experimental noninformative writing
Writing C (Control informative writing)
Control informative writing
Writing D (Control noninformative writing)
Control noninformative writing

Locations

Country Name City State
United States University of North Carolina at Chapel Hill Chapel Hill North Carolina
United States Hackensack University Medical Center Hackensack New Jersey
United States Mount Sinai School of Medicine New York New York

Sponsors (2)

Lead Sponsor Collaborator
University of North Carolina, Chapel Hill American Cancer Society, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Psychological Adjustment At screening, baseline and 3 months following intervention
Secondary Quality of Life At screening, baseline and 3 months following intervention
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