Completed
To Evaluate the Effectiveness of a Patient Self-reported Pain Scoring Tool and a Satisfaction Survey on Cancer Pain Management; Multicenter, Cross-sectional Study
What is being collected
Behavioral Data
Collected from today forward - ProspectiveBehavioral
Who is being recruted
Neurologic Manifestations+2
+ Signs and Symptoms
+ Pathological Conditions, Signs and Symptoms
Over 18 Years
+5 Eligibility Criteria
How is the trial designed
Cohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Observational
Study Start: January 2012
Summary
Principal SponsorJanssen Korea, Ltd., Korea
Last updated: April 11, 2013
Sourced from a government-validated database.Claim as a partner
Study start date: January 1, 2012
Actual date on which the first participant was enrolled.The purpose of this survey is to investigate the usefulness of a patient self-reported scoring tool on patient satisfaction improvement.
Principal SponsorJanssen Korea, Ltd., Korea
Last updated: April 11, 2013
Sourced from a government-validated database.Claim as a partner
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Design Details
587 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Conditions
Criteria
Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsCancer PainPain
Criteria
4 inclusion criteria required to participate
Patients admitted to a hospital for more than 5 days due to cancer pain
Patients for whom their pain managing physicians completed the medical staff's survey
Patients who are able to understand and answer the pain scoring tool questions
Patients who have no experience with the study self-reported pain scoring tool
1 exclusion criteria prevent from participating
Patients who cannot answer the questions due to cognitive impairments
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Treatment Groups
Study Objectives
One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has no location dataSave this study to your profile to know when the location data is available.
CompletedNo study centers