Alternate Title
Basic Trial Information
Objectives
Entry Criteria
Expected Enrollment
Outcomes
Outline
Trial Contact Information
Registry Information
Evaluating Patient Participation in Phase I Clinical Trials
| Phase | Type | Status | Age | Sponsor | Protocol IDs |
|---|---|---|---|---|---|
| No phase specified | Educational/Counseling/Training | Completed | 18 and over | NCI | NCI-02-C-0204 NCT00043030 |
Objectives
- Describe the motivations, perceptions, and expectations of patients enrolled in a phase I clinical trial.
- Assess the influence of age, education, and gender upon the perception of these patients.
- Compare the difference in perceptions, motivations, and expectations of patients who have previously participated in a phase I clinical trial vs those who have not.
- Determine whether patients' perceptions, motivations, and expectations change while enrolled in a phase I clinical trial.
- Validate an interviewer-administered tool measuring the perceptions, motivations, and expectations of these patients.
- Assess patients' perception of the information they were given while enrolled in a phase I clinical trial.
Entry Criteria
Disease Characteristics:
- Enrolled in a phase I clinical trial within the past week
- Signed an informed consent for a phase I trial
Prior/Concurrent Therapy:
Biologic therapy
- Not specified
Chemotherapy
- Not specified
Endocrine therapy
- Not specified
Radiotherapy
- Not specified
Surgery
- Not specified
Other
- Prior participation in a phase I clinical trial allowed
Patient Characteristics:
Age
- 18 and over
Performance status
- Not specified
Life expectancy
- Not specified
Hematopoietic
- Not specified
Hepatic
- Not specified
Renal
- Not specified
Other
- Able to follow basic verbal instructions as witnessed by the investigator or a representative
- Able to understand and speak English as determined by the investigator or a representative
- Access to a telephone
Expected Enrollment
120A total of 120 patients will be accrued for this study within 1 year.
Outcomes
Primary Outcome(s)Patients' perceptions, motivations, and expectations as assessed by survey prior to and 2 months after enrollment on a phase I clinical trial
Influence of age and education on perception as assessed by survey prior to and 2 months after enrollment on a phase I clinical trial
Compare difference between patients who have and who have not previously participated in phase I clinical trials as assessed by survey prior to and 2 months after enrollment on a phase I clinical trial
Changes in patients' perceptions, motivations, and expectations as assessed by survey prior to and 2 months after enrollment on a phase I clinical trial
Validate measurement of patients' perceptions, motivations, and expectations as assessed by survey prior to and 2 months after enrollment on a phase I clinical trial
Patient's perceptions of information given as assessed by survey prior to and 2 months after enrollment on a phase I clinical trial
Influence of gender upon perception as assessed by survey prior to and 2 months after enrollment on a phase I clinical trial
Outline
Patients are interviewed over the phone to evaluate their perceptions, motivations, and expectations of phase I clinical trials. Patients complete a questionnaire comprising 24 questions over 30-45 minutes. Interviews are conducted within 1 week after enrolling in a phase I clinical trial (prior to the first dose of study agent) and then again 2 months later (or at the time the patient stops treatment). The first 10 patients enrolled complete an additional 6 questions over 15 minutes during the first interview to validate the questionnaire, but do not complete a second interview.
Trial Lead Organizations
NCI - Center for Cancer Research
| Arlene Berman, RN, MS, OCN, Principal investigator |
| ||
| Registry Information | ||
| Official Title | Survey Of Patient's Motivations, Perceptions, And Expectations In Phase I Clinical Trials | |
| Trial Start Date | 2002-06-01 | |
| Trial Completion Date | 2009-05-05 | |
| Registered in ClinicalTrials.gov | NCT00043030 | |
| Date Submitted to PDQ | 2002-06-05 | |
| Information Last Verified | 2007-02-06 | |
Note: The purpose of most clinical trials listed in this database is to test new cancer treatments, or new methods of diagnosing, screening, or preventing cancer. Because all potentially harmful side effects are not known before a trial is conducted, dose and schedule modifications may be required for participants if they develop side effects from the treatment or test. The therapy or test described in this clinical trial is intended for use by clinical oncologists in carefully structured settings, and may not prove to be more effective than standard treatment. A responsible investigator associated with this clinical trial should be consulted before using this protocol.
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