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Spots Global Cancer Trial Database for Narrative Medicine for Improving Well-Being in Patients With Gastrointestinal Cancers

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Trial Identification

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

Official Title: Can Narrative Medicine Methods Improve Well-Being in Patients With GI Malignancies

Study ID: NCT06374251

Study Description

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.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

USC / Norris Comprehensive Cancer Center, Los Angeles, California, United States

Contact Details

Name: Eve L Makoff, MD

Affiliation: University of Southern California

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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