Skip to main content
OpenTrials
Completed

NCT Number: NCT02822430

Pain in Psychiatry : Impact on Length of Hospital Stays

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Functionnal unit of psychiatry

Toulouse, 31000, France

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Pain scales

Other
  • Visual analogic scale of pain
  • Pain behaviour scale
  • Short-FormHealth Survey (SF-36)
  • Clinical Global impression
  • Mini International Neuropsychiatric Interview (MINI)

Primary outcomes

  1. Influence of pain on hospitalization stay evaluated with pain visual analogic scale

    Time frame: Day 1

    Multivariate regression analysis

  2. Influence of pain on hospitalization stay evaluated with pain visual analogic scale

    Time frame: Day 7

    Multivariate regression analysis

  3. Influence of pain on hospitalization stay evaluated with pain visual analogic scale

    Time frame: 2 days before patient end of hospitalization

    Multivariate regression analysis

Secondary outcomes

  1. Evaluation of pain in psychiatric population with visual analogic scale of pain

    Time frame: Day 1

  2. Evaluation of pain in psychiatric population with visual analogic scale of pain

    Time frame: Day 7

  3. Evaluation of pain in psychiatric population with visual analogic scale of pain

    Time frame: 2 days before patient end of hospitalization

  4. Evaluation of pain intensity impact on Mini International Neuropsychiatric Interview score

    Time frame: Day 1

  5. Evaluation of pain intensity impact on Mini International Neuropsychiatric Interview score

    Time frame: 2 days before the patient end of hospitalization

  6. Evaluation of gender impact on pain intensity using visual analogic scale of pain

    Time frame: Day 1

  7. Evaluation of gender impact on pain intensity using visual analogic scale of pain

    Time frame: 2 days before the patient end of hospitalization

  8. Evaluation of age impact on pain intensity using visual analogic scale of pain

    Time frame: Day 1

  9. Evaluation of age impact on pain intensity using visual analogic scale of pain

    Time frame: 2 days before the patient end of hospitalization

  10. Evaluation of Mini International Neuropsychiatric Interview score impact on hospitalization stay

    Time frame: Day 1

  11. Evaluation of Mini International Neuropsychiatric Interview score impact on hospitalization stay

    Time frame: 2 days before the patient end of hospitalization

Sponsors and collaborators

Lead sponsor

University Hospital, Toulouse

Other

Registry information

Acronym: D-PSY

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Jul 4, 2016
Registry last updated
Jul 4, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.