Completed
POSITAGProcess-outcome-study in the Context of a Lifestyle Modification Program for Patients With Chronic Pain Conditions
What is being collected
Behavioral Data
Collected from today forward - ProspectiveBehavioral
Who is being recruted
Neurologic Manifestations+2
+ Pain
+ Signs and Symptoms
From 18 to 75 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 2013
Summary
Principal SponsorUniversität Duisburg-Essen
Last updated: September 4, 2015
Sourced from a government-validated database.Claim as a partner
Study start date: January 1, 2013
Actual date on which the first participant was enrolled.see above
Principal SponsorUniversität Duisburg-Essen
Last updated: September 4, 2015
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
200 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.From 18 to 75 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 ManifestationsPainSigns and SymptomsPathological Conditions, Signs and SymptomsChronic Pain
Criteria
4 inclusion criteria required to participate
18-78
diagnosed with any chronic pain condition
physical and mental ability to participate in the program and the study
written informed consent
1 exclusion criteria prevent from participating
participation in any other clinical study focusing on psychological or behavioral intervention
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 1 location
Department of Internal and Integrative Medicine, Kliniken Essen-Mitte
Essen, GermanyOpen Department of Internal and Integrative Medicine, Kliniken Essen-Mitte in Google MapsCompletedOne Study Center