USC / Norris Comprehensive Cancer Center
Los Angeles, California, 90033, United States
NCT Number: NCT06374251
This clinical trial assesses whether narrative medicine methods may improve the sense of well-being among gastrointestinal (GI) (digestive system) cancer patients. Narrative medicine is a clinical approach where providers can use a patient's own narrative (perspective) of their illness to promote healing and resilience. By applying narrative medicine's main tool, close reading, to clinical practice, clinicians learn to listen and attend to patients more deeply. This allows for freer communication and the creation of a healthcare encounter that centers on the psychological and emotional well being of the patient in addition to their medical conditions. Narrative medicine can include close reading, creative or reflective writing, and discussion. These methods may help patients with GI cancer to reflect on their life stories, both inside and outside of their illness experience, and help them gather skills to optimize their well-being.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Los Angeles, California, 90033, United States
PRIMARY OBJECTIVES:
I. To assess the feasibility of implementing narrative medicine tools in serial workshops with patients with malignancy.
II. To determine if narrative medicine interventions improve markers and expressions of well-being.
DESCRIPTIVE OBJECTIVES:
I. To estimate changes in markers and expressions of well-being after 3 sessions of narrative medicine intervention.
II. To determine, through qualitative methods, if patients find benefit from the intervention regarding their well-being.
III. To decide whether to expand these kinds of interventions to a larger study with control group.
OUTLINE:
Patients participate in narrative medicine sessions over 60 minutes once every 2 weeks (Q2W) for 3 sessions.
After completion of study intervention, patients are followed up at 1 and 3 months.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participate in narrative medicine sessions
Other names: Discuss
Ancillary studies
Ancillary studies
Time frame: Up to 3 months
To determine the intervention feasibility, the number of participants who complete the narrative medicine sessions will be tracked.
Time frame: Up to 3 months
Will be evaluated using the Edmonton Symptom Assessment System-Revised Version (ESAS-r). The total score ranges from 0 to 10, with a higher score indicating worse outcomes.
University of Southern California
Other
Can Narrative Medicine Methods Improve Well-Being in Patients With GI Malignancies
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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