ClinicalTrials.Veeva

Menu

Validation of a New Questionnaire Regarding Pain Management

R

Ruhr University of Bochum

Status

Completed

Conditions

Pain

Study type

Observational

Funder types

Other

Identifiers

NCT02266199
VNQI-2012

Details and patient eligibility

About

The study includes operative as well as conservative patients using a questionnaire containing items of pain quality. After having completed the questionnaire, the patient is interviewed by an assistant. By this way the new questionnaire should be validated.

In addition the patient´s personal experiences are included and conservative patients can be compared to operative patients.

Full description

It is validated whether the questions are formulated comprehensively and the patient consequently is able to understand all the different interrogated aspects of the questionnaire.

Exemplarily the patient is asked to express his pain in an analogue scale in various situations and which type of pain they experience (for example headache).

Moreover, it is tested whether there is a relation between the pain and the treatment he receives, and whether the patient expressed the need for additional medication.

Besides, it is asked whether he already took medication before his hospitalisation.

With help of the interview, which is conducted subsequent to the questionnaire, it is verified if the patient understands the aspects. Some of the questions are interrogated in depth by additional questions, for example which type of pain he experiences in which situation.

One important aspect is to find out whether the patient is conscious about his medication.

In order to do so, schedules are used, which are based on the documented patient's history.

Enrollment

350 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Signing the consent form
  • Patients with acute postoperative pain
  • Patients with acute pain with conservative treatment
  • Patients with ≥ 18 years of age

Exclusion criteria

  • Lack of signature of the informed consent
  • All physical and mental impairments which don´t allow the completion of the questionnaire or answering the interview
  • Difficulties with the German language
  • <18 years of age
  • Isolation of patient

Trial design

350 participants in 2 patient groups

conservative patients
Description:
in-patients on pneumology, cardiology, neurology, gastroenterology, endocrinology
operative patients
Description:
inpatient on Traumatology, Plastic Surgery, Cardiothoracic Surgery, Gynecology, Abdominal Surgery

Trial contacts and locations

3

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems