Cancer Clinical Trial
Official title:
Study of Patient Satisfaction With the Cancer Clinical Trial Experience
| Verified date | May 2012 |
| Source | Summa Health System |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | United States: Institutional Review Board |
| Study type | Observational |
The primary objective of this study is to evaluate the quality of the clinical trial
experience of cancer patients participating in cancer research studies through Summa Health
System Hospitals Cancer Research Program by evaluating patient satisfaction regarding
reasons for participating, facility, consent and treatment, personal issues and overall
assessment.
The secondary objective of this study is to determine areas for improvement to make the
patient's clinical trial experience a satisfying and positive journey.
| Status | Completed |
| Enrollment | 100 |
| Est. completion date | May 2012 |
| Est. primary completion date | May 2012 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years to 80 Years |
| Eligibility |
Inclusion Criteria: - Participant must have participated in a clinical trial conducted by the Summa Health System Hospitals Cancer Research Program. - Participant should have been registered for clinical trial participation three months prior to receiving the satisfaction survey. Exclusion Criteria: - Participant has withdrawn consent for clinical trial participation and/or follow up. - Participant has a major medical illness that would prevent completion of the survey. |
Observational Model: Ecologic or Community, Time Perspective: Prospective
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| Summa Health System |
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Evaluation of surveys to determine if there are opportunities for performance and/or quality improvement projects.patient satisfaction regarding reasons for participating, facility, consent and treatment, personal issues and overall assessment. | Survey will be sent to subject 3 months after study registration | No |
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