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Narrative Medicine for Improving Well-Being in Patients With Gastrointestinal Cancers

Not Applicable
Recruiting
Conditions
Malignant Digestive System Neoplasm
Interventions
Procedure: Discussion
Other: Interview
Other: Survey Administration
Registration Number
NCT06374251
Lead Sponsor
University of Southern California
Brief Summary

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.

Detailed Description

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.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
10
Inclusion Criteria
  • Patients with diagnosis of gastrointestinal malignancy actively receiving infusional therapy for cancer.
  • Age >= 18 years.
  • English speaking with ability to participate in reading and writing questionnaires and implementation tools.
  • Performance Status =< Eastern Cooperative Oncology Group (ECOG) 3.
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Exclusion Criteria
  • Altered mental status or other cognitive impairment, organic or drug induced that would limit ability to participate in the evaluation.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Supportive Care (narrative medicine sessions)DiscussionPatients participate in narrative medicine sessions over 60 minutes Q2W for 3 sessions.
Supportive Care (narrative medicine sessions)InterviewPatients participate in narrative medicine sessions over 60 minutes Q2W for 3 sessions.
Supportive Care (narrative medicine sessions)Survey AdministrationPatients participate in narrative medicine sessions over 60 minutes Q2W for 3 sessions.
Primary Outcome Measures
NameTimeMethod
Number of participants who complete the narrative medicine sessionsUp to 3 months

To determine the intervention feasibility, the number of participants who complete the narrative medicine sessions will be tracked.

Change in well-being scoresUp 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.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

USC / Norris Comprehensive Cancer Center

🇺🇸

Los Angeles, California, United States

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