Outlook: An Intervention to Improve Quality of Life in Serious Illness
This is a pilot randomized control trial to evaluate the feasibility of the Outlook
intervention. 36 veterans with advanced cancer, CHF or COPD will be randomly assigned to one
of three intervention groups and complete a brief battery of pre-test measures. Subjects in
the first group ("treatment") will meet with a facilitator three times for a period of 45
min-1 hour. In the first session, subjects will be asked to discuss issues related to life
review. In the second session, participants will be asked to speak in more depth about
issues such as regret, forgiveness and things left undone, In the final session, subjects
will focus on heritage and legacy. The subjects in the second group ("attention control")
will meet with a facilitator three times for a period of 45 min- 1 hour and listen to a
non-guided relaxation CD. The third group of participants ("true control") will be exposed
to no intervention or attention control. One week and two weeks later, participants in all
groups will receive post-test measures administered by a blinded interviewer.
Interventional
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label
Quality of life
8 weeks
No
Karen E. Steinhauser, PhD
Principal Investigator
Durham VA Medical Center HSR&D COE
United States: Federal Government
IAD 07-162
NCT00784095
December 2008
May 2009
Name | Location |
---|---|
Durham VA Medical Center HSR&D COE | Durham, North Carolina 27705 |