Psychosocial Evaluation Prior to Lung Transplantation (EVALUT)

June 9, 2016 updated by: Hannover Medical School

Standardized Evaluation of Psychosocial Functioning in Patients Awaiting Lung Transplantation

In a prospective longitudinal cohort study we aim at investigating the extent to which pre-transplant psychosocial levels of functioning predict the medical and psychosocial outcomes of lung transplantation. There is evidence that e.g. persistently elevated depressive symptoms are associated with reduced survival after lung transplantation

Study Overview

Status

Unknown

Detailed Description

There is ample evidence that there are high rates of anxiety and depression among patients with end-stage lung disease. In addition, psychological dysfunction and distress seem to be especially prevalent in patients awaiting lung transplantation. Even though patients benefit from the transplant procedure with respect to long-term health-related quality of life (HRQoL), they also face significant challenges in terms of psychosocial adjustment after the transplantation. There is evidence that e.g. persistently elevated depressive symptoms are associated with reduced survival after lung transplantation.

Currently, the screening process to help select among candidates for organ transplant typically involves considering a variety of psychosocial factors. However, it remains somewhat unclear which criteria are considered important in these evaluations, how differences in various aspects of psychosocial functioning are weighed in making the ultimate decision on the suitability of a patient for transplantation, and the extent to which pretransplant psychosocial characteristics predict the medical and psychosocial outcomes of the procedure. Standardized psychometric instruments with proven reliability and validity can prevent the danger of personal bias in the selection of candidates for transplantation. In addition, structured psychometric instruments can help to identify patients with multiple care needs and can support the development of psychosocial interventions designed to increase quality of life and to decrease the risk of a less favorable transplant outcome through modifying the factors that might place patients at risk.

In a longitudinal prospective cohort study, psychosocial functioning will be assessed at multiple time points both before and after lung transplantation. Assessment of psychosocial functioning will be conducted using a validated, structured interview which allows a comprehensive evaluation of the level of adjustment in 10 aspects of psychosocial functioning - the Transplant Evaluation Rating Scale (TERS) - and standardized self-report instruments. The TERS has shown to be an important and significant predictor of several facets of somatic and psychosocial outcomes e.g. in patients after liver transplantation, left ventricular assist device implantation, and hematopoietic stem cell transplantation.

For each patient, a face-to-face psychosomatic evaluation 1 year after Transplantation will take place during a routine clinical assessments at the Department of Respiratory Medicine.

The following outcome parameters will be assessed:

  • Mental disorders (current)
  • Psychological processing of lung transplantation (including organ integration and the patient's relationship with the donor, chronic stress/psychological distress and the emotional effects of transplantation/immunosuppression
  • Return to work one year after lung transplantation
  • Psychological interventions during the first postoperative year
  • Intake of (new) psychotropic medication during the first postoperative year

Study Type

Observational

Enrollment (Anticipated)

200

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

All patients presenting for evaluation at the interdisciplinary lung transplant outpatient clinic of Hannover Medical School or already listed for lung Transplantation and being in Treatment at Hannover Medical School

Description

Inclusion Criteria:

  • patients listed for lung Transplantation (including combined Transplantation) or who are evaluated at the interdisciplinary lung transplant outpatient clinic
  • regular post-transplant visits at the Department of Respiratory Medicine
  • informed consent

Exclusion Criteria:

  • Age below 18 years
  • lacking German language skills
  • severe cognitive disability
  • re-do Transplantation
  • colonization with pan- or multi-resistant organisms with Need for isolation

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
change in survival status after lung transplantation
Time Frame: assessments at 1, 3, 6 and 12 month after lung transplantation
number of days survived during first post-operative year
assessments at 1, 3, 6 and 12 month after lung transplantation

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
duration of hospitalization after lung transplantation
Time Frame: assessments at 1, 3, 6 and 12 month after lung transplantation
number of days of hospitalization during first post-operative year
assessments at 1, 3, 6 and 12 month after lung transplantation
change in adherence during the first post-operative year
Time Frame: assessments at 1, 3, 6 and 12 month after lung transplantation
mean composite adherence score to immunosuppressants (IS) based on multiple clinical ratings and IS trough levels during first post-operative year
assessments at 1, 3, 6 and 12 month after lung transplantation
change from baseline quality of life to one year post-transplantation
Time Frame: once before admission to waiting list and 12 month after lung transplantation
Change in self-rated multidimensional quality of life
once before admission to waiting list and 12 month after lung transplantation
change in quality of life during first post-operative year
Time Frame: 1, 3, 6 and 12 month after lung transplantation
mean self-rated multidimensional quality of life based on multiple assessments during first post-operative year
1, 3, 6 and 12 month after lung transplantation
change from baseline psychological distress (questionnaire) to one year post-transplantation
Time Frame: once before admission to waiting list and 12 month after lung transplantation
change in levels of self-rated anxiety and depressive symptoms
once before admission to waiting list and 12 month after lung transplantation
change in psychological distress (questionnaire) during first post-operative year
Time Frame: 1, 3, 6 and 12 month after lung transplantation
mean levels of self-rated anxiety and depressive symptoms based on multiple assessments during first post-operative year
1, 3, 6 and 12 month after lung transplantation
mental disorders
Time Frame: 12 month after lung transplantation
number and kind of current mental disorders at one year after lung transplantation
12 month after lung transplantation
integration of transplant in own Body Image (questionnaire)
Time Frame: 12 month after lung transplantation
Quality of psychological processing of lung Transplantation and Feelings towards donor one year after lung transplantation
12 month after lung transplantation
psychological interventions
Time Frame: 12 month after lung transplantation
number and kind of psychosocial interventions during first post-operative year
12 month after lung transplantation
psychotropic medication
Time Frame: 12 month after lung transplantation
kind and intake of (new) psychotropic medication during first post-operative year
12 month after lung transplantation
change from baseline comorbidity to one year post-Transplantation (clinical Rating)
Time Frame: once before admission to waiting list and 12 month after lung transplantation
change in kind, number and degree of comorbid conditions
once before admission to waiting list and 12 month after lung transplantation
Change in comorbidity (clinical Rating)
Time Frame: 1, 3, 6 and 12 month after lung transplantation
mean number and degree of comorbid conditions during first post-operative year
1, 3, 6 and 12 month after lung transplantation

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Jens Gottlieb, Prof. Dr., Hannover Medical School
  • Principal Investigator: Martina de Zwaan, Prof. Dr., Hannover Medical School

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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

January 1, 2016

Primary Completion (Anticipated)

December 1, 2018

Study Completion (Anticipated)

December 1, 2018

Study Registration Dates

First Submitted

April 28, 2016

First Submitted That Met QC Criteria

June 9, 2016

First Posted (Estimate)

June 15, 2016

Study Record Updates

Last Update Posted (Estimate)

June 15, 2016

Last Update Submitted That Met QC Criteria

June 9, 2016

Last Verified

May 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • DZL BREATH-EVALUT

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.

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