Clinical Trial Details
— Status: Withdrawn
Administrative data
NCT number |
NCT04235218 |
Other study ID # |
REG-081-2019 |
Secondary ID |
|
Status |
Withdrawn |
Phase |
|
First received |
|
Last updated |
|
Start date |
May 20, 2022 |
Est. completion date |
February 1, 2023 |
Study information
Verified date |
June 2021 |
Source |
Zealand University Hospital |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Observational
|
Clinical Trial Summary
We wish to clarify whether we can demonstrate a correlation between scores in Brief-IPQ and
the effect of treatment in patients referred to our department, Interdisciplinary Pain Center
Zealand University Hospital Koege, Denmark. The purpose is to outline whether we can use
Brief-IPQ with Chronic Pain disorders and thereby detect those of our referred patients who
are at risk for poor treatment response in an early state. In these cases, we can offer
psychological intervention at the beginning of the course of treatment, in order to optimize
the conditions for patients and achieve an optimal treatment effect.
Description:
Chronic pain conditions are frequent in the danish population. More than 1.2 million Danes
over the age of 16 are living with chronic pain. Chronic pain affects the health-related
quality of life and functioning and is associated with reduced work ability, lost earnings
and disability. At the Interdisciplinary Pain Center Zealand University Hospital Koege,
Denmark, patients with chronic pain are received and treated based on the Bio-Psycho-Social
Pain Model. The treatment of patients with complex chronic non-malignant pain can be
complicated by psychological and / or social factors. The need for a screening of
psychological factors in connection with the examination and planning of the pain management
in the Interdisciplinary Pain Center is obvious as the patient's perception of illness and
expectation of treatment have been shown to play a role in the treatment response. The Brief
Illness Perception Questionnaire (Brief-IPQ) provides a quick assessment of the patient's
disease perception and expectation of treatment and has proved useful in clinical practice.
In this study, a Danish version of Brief-IPQ is used, which initially was taken from
https://www.uib.no. Items as stated in research by L. van Oort et al (2011) have been adapted
to the Danish version. A copy of the latest version can be obtained from Interdisciplinary
Pain Center Zealand University Hospital Koege, Denmark.
The Study:
The study is designed as a prospective observational study of the correlation between
Brief-IPQ and pain-related and demographic data in patients referred to Interdisciplinary
Pain Center Zealand University Hospital Køge, Denmark. Brief IPQ and PainData (which is a
database which records the well-being of Danish pain patients and operated by "Danske
Regioner" and Odense University Hospital) is measured at the start of treatment and after 6
months. They will consists of items such as; Married or cohabitant, Vocational training,
Educational length, Occupational status. There will furthermore be an assessment of pain type
such as; nociceptive / neurogenic / generalized / visceral / other as well as the duration of
symptoms and treatment with opioids: +/-, equipotent daily doses. Additionally we focus on
Pain intensity (NRS) from Paindata, Psychological profile (from Paindata): anxiety,
depression, stress, fear-avoidance, self-efficacy and the following changes before and after
six months of treatment:
Inclusion:
All patients referred to Interdisciplinary Pain Center Zealand University Hospital Koege,
Denmark and start the treatment from the start date of the study can be included in the study
provided:
- Age over 18 years
- Understands and speaks Danish
Exclusion:
Patients who meet one of the following criteria are not eligible for inclusion in this study:
- Patients who do not have sufficient cognitive skills to complete the form (Brief-IPQ)
- Patients who cannot cooperate to complete the form (Brief-IPQ)
- Patients who submit invalid or illegible answers (Brief-IPQ)
Number of patients needed:
60 patients with complete data or number included as of May 1, 2020. Time schedule:
Collection of data: start February 1.2020 End: when complete data has been obtained from 60
patients, or no later than 1.12.2020
Ethical aspects:
All information will be treated confidentially and all data will be anonymized by a
secretary. The Investigator will keep an identification list of all patients who have been
included. This list will include the patient's full name and CPR number. Collected data will
be recorded in a Case Report Form. The results will be stored and analyzed using a computer
and the anonymity of the patients will be preserved and local data law will be observed. Data
will be stored in accordance with existing regulations. Data is stored in anonymized form and
correlation and regression analysis will be performed after 6 months. The study is conducted
in accordance with applicable clinical trial rules. Investigators are responsible for the
handling and archiving of data in accordance with applicable rules in addition to the Act on
the Processing of Personal Data and the Health Act. Data belong to the investigators. The
project has been reported to the local ethic committee.