- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02559375
PAIN-LESS: Understanding and Alleviating Pain for Cancer Patients in Academic and Community Hospitals
July 22, 2019 updated by: Abramson Cancer Center of the University of Pennsylvania
This study will increase knowledge of patient preferences for pain treatments, and improve the ability to meet patients pain management needs.
This study will assess patient attitudes towards underutilized treatments and identify technologies to increase awareness of such treatments.
This study also demonstrate the feasibility of using the Penn Cancer Network in future clinical and cancer control research and better understand how to effectively raise patients awareness of supportive cancer services.
Study Overview
Study Type
Observational
Enrollment (Actual)
466
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Pennsylvania
-
Philadelphia, Pennsylvania, United States, 19104
- Abramson Cancer Center of the University of Pennsylvania
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Cancer Patients
Description
Inclusion Criteria:
- Age 18 or older; Have a primary diagnosis of cancer;
- Have a Karnofsky functional score of 60 or greater (i.e. ambulatory);
- Understand written English;
- Verbally indicate to the RA/RN that they feel physically well enough to complete a survey at the time of approach;
- Report experiencing nonzero pain (on a scale of 0-10) in the last seven days
Exclusion Criteria:
- An inability to understand the requirements of the survey
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Number of subjects providing completed surveys
Time Frame: 1 year
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
September 1, 2014
Primary Completion (Actual)
September 30, 2015
Study Completion (Actual)
September 30, 2015
Study Registration Dates
First Submitted
June 23, 2015
First Submitted That Met QC Criteria
September 23, 2015
First Posted (Estimate)
September 24, 2015
Study Record Updates
Last Update Posted (Actual)
July 23, 2019
Last Update Submitted That Met QC Criteria
July 22, 2019
Last Verified
July 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- UPCC 26914
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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