Pain in Psychiatry : Impact on Length of Hospital Stays (D-PSY)

June 29, 2016 updated by: University Hospital, Toulouse
For several decades, authors are interested in the existence and meaning of painful symptoms in a population of psychiatric inpatients. But, to date, studies specifically focused on the impact of pain in patient populations in psychiatric hospitals are few. More recently, a review of the literature highlights the difficulties of evaluation of pain in populations of psychiatric patients but also the complex interrelationships between painful symptoms and psychiatric diseases. The first national survey conducted among 172 health which evaluate pain and its management in the field of psychiatry concluded on the need to develop research in this area.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Pain in all the populations remains a major public health issue. Patients with mental illness consult less their general practitioners while they have an increased risk of physical disease. In addition, they have a net reduction in life expectancy due to their mental illness, living conditions and drug treatments.

In this particular population, doctors faces especially difficulties assessment and treatment of pain. Indeed, there is for example in some of these patients difficulties to express that pain.

These painful events make more complex the care of hospitalized patients (eg interrelationship between pain complaints and psychiatric symptoms) and seem to lengthen their hospital stay. This is not without consequences as long as hospitalizations represent an obstacle to the patients psychosocial rehabilitation (installation of daytime activities, project work rehabilitation, development of social network ...) and impair their quality of life.

And for the patients with psychiatric disorders some points can be noticed :

  • An increased risk of physical disease
  • Warning signs like pain poorly known and poorly evaluated ... and poorly supported
  • The presence of the pain seems to lengthen the hospital stay
  • An extension of the hospital stay, which represent an obstacle to the psychosocial rehabilitation This research project is to test if the presence of a painful complaint among psychiatric inpatients is associated lengthening of the hospitalization duration.

The secondary objectives of this study are:

  • To measure the prevalence of painful complaint in this specific population,
  • To examine the evolution of pain during hospitalization.
  • Identify factors influencing the relationship between pain and length of stay
  • To identify if the intensity of the psychiatric illness is associated with pain intensity measured

Confirmation of these objectives would lead to a better understanding of the factors influencing psychiatric hospital stays and thus more efficient management of health resources.

In addition, the present study will well identify and implement standardized assessments of pain for these patients.

For these patients the interest is important because they can be in great difficulty to express a painful complaint. These people have often difficulties to communicate, and live in a sometimes precarious environment and severity of disorders reduce their access to care.

This approach is part of a comprehensive approach taking account of the psychiatric and somatic disorders in a very vulnerable population.

Study Type

Observational

Enrollment (Actual)

137

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

      • Toulouse, France, 31000
        • Functionnal unit of psychiatry

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

Non-Probability Sample

Study Population

Patients with psychiatric disorders

Description

Inclusion Criteria:

  • Patient eighteen years old
  • Patient hospitalized in psychiatric service at Toulouse University Hospital
  • Informed consent signed

Exclusion Criteria:

  • Patient treated with maintenance sismotherapy

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Patients

Patients with psychiatric disorders will be assessed using five evaluation of pain scales :

  • Visual analogic scale pain
  • Pain behaviour scale
  • Short-FormHealth Survey (SF-36)
  • Global Clinical Impression (GCI) for severity and improvement
  • Mini International Neuropsychiatric Interview (MINI)
  • Visual analogic scale of pain
  • Pain behaviour scale
  • Short-FormHealth Survey (SF-36)
  • Clinical Global impression
  • Mini International Neuropsychiatric Interview (MINI)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Influence of pain on hospitalization stay evaluated with pain visual analogic scale
Time Frame: Day 1
Multivariate regression analysis
Day 1
Influence of pain on hospitalization stay evaluated with pain visual analogic scale
Time Frame: Day 7
Multivariate regression analysis
Day 7
Influence of pain on hospitalization stay evaluated with pain visual analogic scale
Time Frame: 2 days before patient end of hospitalization
Multivariate regression analysis
2 days before patient end of hospitalization

Secondary Outcome Measures

Outcome Measure
Time Frame
Evaluation of pain in psychiatric population with visual analogic scale of pain
Time Frame: Day 1
Day 1
Evaluation of pain in psychiatric population with visual analogic scale of pain
Time Frame: Day 7
Day 7
Evaluation of pain in psychiatric population with visual analogic scale of pain
Time Frame: 2 days before patient end of hospitalization
2 days before patient end of hospitalization
Evaluation of pain intensity impact on Mini International Neuropsychiatric Interview score
Time Frame: Day 1
Day 1
Evaluation of pain intensity impact on Mini International Neuropsychiatric Interview score
Time Frame: 2 days before the patient end of hospitalization
2 days before the patient end of hospitalization
Evaluation of gender impact on pain intensity using visual analogic scale of pain
Time Frame: Day 1
Day 1
Evaluation of gender impact on pain intensity using visual analogic scale of pain
Time Frame: 2 days before the patient end of hospitalization
2 days before the patient end of hospitalization
Evaluation of age impact on pain intensity using visual analogic scale of pain
Time Frame: Day 1
Day 1
Evaluation of age impact on pain intensity using visual analogic scale of pain
Time Frame: 2 days before the patient end of hospitalization
2 days before the patient end of hospitalization
Evaluation of Mini International Neuropsychiatric Interview score impact on hospitalization stay
Time Frame: Day 1
Day 1
Evaluation of Mini International Neuropsychiatric Interview score impact on hospitalization stay
Time Frame: 2 days before the patient end of hospitalization
2 days before the patient end of hospitalization

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Laurent SCHMITT, PHD, MD, University Hospital, Toulouse

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

April 1, 2014

Primary Completion (ACTUAL)

July 1, 2015

Study Completion (ACTUAL)

July 1, 2015

Study Registration Dates

First Submitted

June 21, 2016

First Submitted That Met QC Criteria

June 29, 2016

First Posted (ESTIMATE)

July 4, 2016

Study Record Updates

Last Update Posted (ESTIMATE)

July 4, 2016

Last Update Submitted That Met QC Criteria

June 29, 2016

Last Verified

June 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • RC31-13-7017

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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.

Clinical Trials on Pain

Clinical Trials on Pain scales

Subscribe