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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00768976
Other study ID # Clinical trial experience
Secondary ID
Status Completed
Phase N/A
First received October 7, 2008
Last updated May 22, 2012
Start date October 2008
Est. completion date May 2012

Study information

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

Clinical Trial Summary

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.


Recruitment information / eligibility

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- Participant has withdrawn consent for clinical trial participation and/or follow up.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.

Study Design

Observational Model: Ecologic or Community, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Summa Health System

Outcome

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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