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The Exceptional Patient in Cancer Care

The Exceptional Patient in Cancer Care

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00543153
Enrollment
13
Registered
2007-10-12
Start date
2007-08-31
Completion date
2010-08-31
Last updated
2012-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Advanced Cancer

Keywords

Advanced Cancer, Exceptional Patient, Cancer Care, Interview

Brief summary

The objectives of this study is to conduct a multicenter, dual country (United States and Israel), study examining the experience of patients with cancer that were considered by their physicians as having exceptional course of survival related to their specific disease state. The primary aim of the study is to develop a detailed description of patients' experience of an exceptional disease course. The secondary aim is to define the content domain for assessment and measurement of exceptional disease course in patients with cancer and identify lessons learned from these exceptional patients that can be a base for future studies to benefit others.

Detailed description

The investigators of this study are exploring the experience of people with cancer who are considered by their physicians as having an exceptional course of disease - people who have defied the odds and remain well despite the severity of the original diagnosis. Participation in this study is completely voluntary. Lessons learned from recorded experience(s) may be helpful to other patients and can be a basis for future studies that may benefit other patients. To participate in this important study is simple and not time consuming. You will have only one face-to-face or telephone interview with a research assistant. During the interview you will simply be asked to describe your perspective, thoughts, and behaviors that you think are related to your disease course and lessons that you think others may gain benefit from. The interview will last about one hour and will be conducted at a time that is convenient for you. If you agree to participate a research assistant will schedule a time for a recorded interview by phone or if possible at a location convenient to you. The interviews will be taped and transcribed. All recorded interviews will be retained for a minimum of 6 years.

Interventions

BEHAVIORALInterview

Interview lasting approximately 30-45 minutes.

Sponsors

M.D. Anderson Cancer Center
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. 18 years of age or older 2. Ability to speak and read English with patients residing in the US, ability to speak and read Hebrew with patients residing in Israel. 3. Diagnosis of cancer confirmed by pathology. 4. Exceptional disease course as identified by patients' physician, in terms of survival and unusual disease course that is appropriately medically documented. 5. Consent to participate in this study.

Exclusion criteria

1. Inability to understand the intent of the study. 2. Medical condition that would preclude participation in an interview session lasting 30-45 minutes. 3. Diagnosis of active psychosis or severe cognitive impairment confirmed by the patient's attending physician.

Design outcomes

Primary

MeasureTime frame
Qualitative Data Collection: Patients' Experience of Exceptional Disease Course2 Years

Countries

Israel, United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026