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Impact of a Systematic Palliative Care on Quality of Life, in Advanced Idiopathic Pulmonary Fibrosis. (PALIF)

Primary Purpose

Idiopathic Pulmonary Fibrosis

Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Supportive care
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Idiopathic Pulmonary Fibrosis focused on measuring idiopathic pulmonary fibrosis, palliative care

Eligibility Criteria

41 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age> 40 years
  • Patient with confirmed diagnosis of IPF according to the American Thoracic Society (ATS) / European Respiratory Society (ERS) / Japanese Respiratory Society (JRS) / Latin American Thoracic Association (ALAT) criteria. The patient may be included regardless of the date of diagnosis.
  • Advanced IPF with Forced Vital Capacity (FVC) <50%" of predicted value and / or Diffusing capacity for carbon monoxide ((DLCO) <30% of predicted value or inability to achieve the Functional Respiratory Investigations (EFR) due to respiratory severity. EFR dated less than 3 months.
  • Absence of argument for acute or subacute exacerbation in the last 6 months.
  • Patient who can be followed in ambulatory consultation/ outpatient consultation.
  • Informed consent signed (signed by the patient or in the presence of a third party for patients who are poorly fluent in French).
  • Affiliation to the social security system.

Exclusion Criteria:

  • Patient unable to respond to quality of life questionnaires.
  • Inability (physical or mental) to give a written informed consent.
  • Acute exacerbation of fibrosis in the previous 6 months.
  • Patient eligible for a pulmonary transplant.
  • Participation in other therapeutic trial
  • Patient cannot be followed in ambulatory consultation.
  • Patient under trustee

Sites / Locations

  • Centre Hospitalier Robert Ballanger
  • Hôpital AvicenneRecruiting
  • Centre Hospitalier de Versailles Andre Mignot
  • Hôpital LOUIS PRADELRecruiting
  • Hôpital NORD
  • Hôpital MARC JACQUETRecruiting
  • Hôpital GEORGES POMPIDOU (HEGP)
  • Hôpital Tenon
  • Hôpital PontchaillouRecruiting
  • Hôpital DELAFONTAINE
  • Hôpital LARREY

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Experimental

standard

Arm Description

Supportive care, systematic and joint to pneumological consultation, monthly, starting at M0 and continuing up to M6.

pneumological consultation performed at M0, M3 and M6

Outcomes

Primary Outcome Measures

The benefit of a systematic, formalized and joint intervention of a palliative intervention staff and a chest physician team on quality of life, evaluated after 6 months by the Short Form (36) Health Survey.
The Short Form (36) Health Survey is a 36-item, patient-reported survey of patient health. The Short Form (36) Health Survey consists of eight scaled scores, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability i.e., a score of zero is equivalent to maximum disability and a score of 100 is equivalent to no disability. The eight sections are: vitality, physical functioning, bodily pain, general health perceptions, physical role functioning, emotional role functioning, social role functioning, mental health. This score has already been used for IPF

Secondary Outcome Measures

The benefit of the systematic, formalized and joint intervention of a supportive care and a pneumologist team on the benefit of the systematic, formalized and joint intervention of a supportive care and a pneumologist team on Mood and depression
evaluated by the Hospital Anxiety and Depression questionnaire. Understanding of diagnosis and therapeutic objectives, frequency of drafting of advance directives Respiratory symptoms (dyspnea) The course of care, the use of palliative care stays and the duration of hospital stays (number and duration of hospitalizations). Overall survival and place of death.
The benefit of the systematic, formalized and joint intervention of a supportive care and a pneumologist team on Understanding of diagnosis and therapeutic objectives, frequency of drafting of advance directives.
the benefit of the systematic, formalized and joint intervention of a supportive care and a pneumologist team on Understanding of diagnosis and therapeutic objectives, frequency of drafting of advance directives will be evaluated by the illness understanding questionnaire.
The benefit of the systematic, formalized and joint intervention of a supportive care and a pneumologist team on Respiratory symptoms (dyspnea)
The benefit of the systematic, formalized and joint intervention of a supportive care and a pneumologist team on Respiratory symptoms (dyspnea) will be evaluated by St George's respiratory questionnaire (SGRQ) and Transition Dyspnea Index (TDI)
The benefit of the systematic, formalized and joint intervention of a supportive care and a pneumologist team on the course of care.
the benefit of the systematic, formalized and joint intervention of a supportive care and a pneumologist team on the course of care, the use of palliative care stays and the duration of hospital stays (number and duration of hospitalizations)
The benefit of the systematic, formalized and joint intervention of a supportive care and a pneumologist team on the Overall survival.
the benefit of the systematic, formalized and joint intervention of a supportive care and a pneumologist team on the Overall survival measured between inclusion and date of death or last news.
Carry out a medico-economic study evaluating the incremental cost-utility and cost-effectiveness ratio (overall survival criterion)
This outcome is evaluated by the medico-economic questionnaire : EuroQol five dimensions questionnaire (EQ-5D)

Full Information

First Posted
July 4, 2017
Last Updated
January 24, 2018
Sponsor
Assistance Publique - Hôpitaux de Paris
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1. Study Identification

Unique Protocol Identification Number
NCT03229343
Brief Title
Impact of a Systematic Palliative Care on Quality of Life, in Advanced Idiopathic Pulmonary Fibrosis.
Acronym
PALIF
Official Title
Impact of a Systematic Palliative Care on Quality of Life, in Advanced Idiopathic Pulmonary Fibrosis (IPF). A Randomized Multi-center Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
July 2017
Overall Recruitment Status
Unknown status
Study Start Date
December 4, 2017 (Actual)
Primary Completion Date
February 2020 (Anticipated)
Study Completion Date
February 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Idiopathic pulmonary fibrosis (IPF) is a rare and severe disease with a survival median between 2 and 4 years which leads to a profound alteration of the quality of life. In thoracic oncology, the systematic and early intervention of a palliative care team result in an improvement of quality of life for patients. In the princeps study published in 2010, the early intervention of a dedicated palliative care team was compared to standard care in a randomized trial of 150 patients and shows a significant improvement : (i) of quality of life (main objective), (ii) of depression scores and even overall survival (11.6 months vs. 8.9 months, P = 0.02), (iii) a benefit in terms of understanding the diagnosis and therapeutic goals (3), (iv) diminution of adapted hospitalization in end of life (in emergency or not). Considering some analogy points between IPF and advanced lung cancer (prognosis, respiratory symptom, psychological burden), it seemed reasonable to assume that the joint systematic intervention of chest physician and palliative care team may provide a significant benefit in terms of quality of life for patients with severe IPF.
Detailed Description
Idiopathic pulmonary fibrosis (IPF) is a rare and severe disease with a survival median between 2 and 4 years which leads to a profound alteration of the quality of life. This alteration results from different consequences of the IPF: progressive shortness of breath, irritative cough refractory to treatments, exhaustion, limitation of activity, social isolation, and psychic consequences such as fear, anxiety and depression. The only current curative treatment of the disease is pulmonary transplantation, but it's only feasible for a minority of patients. Anti-fibrotic drugs, such as pirfenidone and nintedanib, are likely to slow the progression of IPF but have no impact on patients' quality of life. The symptomatic treatment aimed at relieving respiratory discomfort and the patient's quality of life is therefore fundamental, and the IPF meets in many ways the challenges of lung cancer. In thoracic oncology, the systematic and early intervention of a palliative care team result in an improvement of quality of life for patients. In the princeps study published in 2010, the early intervention of a dedicated palliative care team was compared to standard care in a randomized trial of 150 patients and shows a significant improvement : (i) of quality of life (main objective), (ii) of depression scores and even overall survival (11.6 months vs. 8.9 months, P = 0.02), (iii) a benefit in terms of understanding the diagnosis and therapeutic goals (3), (iv) diminution of adapted hospitalization in end of life (in emergency or not). Considering some analogy points between IPF and advanced lung cancer (prognosis, respiratory symptom, psychological burden), it seemed reasonable to assume that the joint systematic intervention of chest physician and palliative care team may provide a significant benefit in terms of quality of life for patients with severe IPF. Objective: To investigate the benefit on quality of life, evaluated after 6 months, of a systematic, formalized and joint intervention of a palliative intervention staff and a chest physician team compared to standard care for patients with severe IPF. Secondary endpoints To evaluate the benefit of the systematic, formalized and joint intervention of a palliative care team and a chest physician team on: Mood and depression Understanding of diagnosis and therapeutic objectives, frequency of drafting of advance directives regarding end-of-life Respiratory symptoms (cough and dyspnea) The course of care, the use of palliative care stays and the duration of hospital stays (number and duration of hospitalizations). Overall survival and place of death. Carry out a medico-economic study evaluating the incremental cost-utility and cost-effectiveness ratio (overall survival criterion)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Idiopathic Pulmonary Fibrosis
Keywords
idiopathic pulmonary fibrosis, palliative care

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Experimental arm : supportive care, systematic and joint to pneumological consultation, monthly, starting at M0 and continuing up to M6. Non interventionnel arm: only pneumological consultation performed at M0, M3 and M6.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Experimental
Arm Type
Experimental
Arm Description
Supportive care, systematic and joint to pneumological consultation, monthly, starting at M0 and continuing up to M6.
Arm Title
standard
Arm Type
No Intervention
Arm Description
pneumological consultation performed at M0, M3 and M6
Intervention Type
Other
Intervention Name(s)
Supportive care
Intervention Description
supportive care, systematic and joint to pneumological consultation, monthly, starting at M0 and continuing up to M6.
Primary Outcome Measure Information:
Title
The benefit of a systematic, formalized and joint intervention of a palliative intervention staff and a chest physician team on quality of life, evaluated after 6 months by the Short Form (36) Health Survey.
Description
The Short Form (36) Health Survey is a 36-item, patient-reported survey of patient health. The Short Form (36) Health Survey consists of eight scaled scores, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability i.e., a score of zero is equivalent to maximum disability and a score of 100 is equivalent to no disability. The eight sections are: vitality, physical functioning, bodily pain, general health perceptions, physical role functioning, emotional role functioning, social role functioning, mental health. This score has already been used for IPF
Time Frame
at 6 months after inclusion
Secondary Outcome Measure Information:
Title
The benefit of the systematic, formalized and joint intervention of a supportive care and a pneumologist team on the benefit of the systematic, formalized and joint intervention of a supportive care and a pneumologist team on Mood and depression
Description
evaluated by the Hospital Anxiety and Depression questionnaire. Understanding of diagnosis and therapeutic objectives, frequency of drafting of advance directives Respiratory symptoms (dyspnea) The course of care, the use of palliative care stays and the duration of hospital stays (number and duration of hospitalizations). Overall survival and place of death.
Time Frame
at 3 and 6 months after inclusion
Title
The benefit of the systematic, formalized and joint intervention of a supportive care and a pneumologist team on Understanding of diagnosis and therapeutic objectives, frequency of drafting of advance directives.
Description
the benefit of the systematic, formalized and joint intervention of a supportive care and a pneumologist team on Understanding of diagnosis and therapeutic objectives, frequency of drafting of advance directives will be evaluated by the illness understanding questionnaire.
Time Frame
at 3 and 6 months after inclusion
Title
The benefit of the systematic, formalized and joint intervention of a supportive care and a pneumologist team on Respiratory symptoms (dyspnea)
Description
The benefit of the systematic, formalized and joint intervention of a supportive care and a pneumologist team on Respiratory symptoms (dyspnea) will be evaluated by St George's respiratory questionnaire (SGRQ) and Transition Dyspnea Index (TDI)
Time Frame
at 3 and 6 months after inclusion
Title
The benefit of the systematic, formalized and joint intervention of a supportive care and a pneumologist team on the course of care.
Description
the benefit of the systematic, formalized and joint intervention of a supportive care and a pneumologist team on the course of care, the use of palliative care stays and the duration of hospital stays (number and duration of hospitalizations)
Time Frame
at 3 and 6 months after inclusion
Title
The benefit of the systematic, formalized and joint intervention of a supportive care and a pneumologist team on the Overall survival.
Description
the benefit of the systematic, formalized and joint intervention of a supportive care and a pneumologist team on the Overall survival measured between inclusion and date of death or last news.
Time Frame
between inclusion and date of death or last news. (survival follow-up visit at month 12)
Title
Carry out a medico-economic study evaluating the incremental cost-utility and cost-effectiveness ratio (overall survival criterion)
Description
This outcome is evaluated by the medico-economic questionnaire : EuroQol five dimensions questionnaire (EQ-5D)
Time Frame
at 3 and 6 months after inclusion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
41 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age> 40 years Patient with confirmed diagnosis of IPF according to the American Thoracic Society (ATS) / European Respiratory Society (ERS) / Japanese Respiratory Society (JRS) / Latin American Thoracic Association (ALAT) criteria. The patient may be included regardless of the date of diagnosis. Advanced IPF with Forced Vital Capacity (FVC) <50%" of predicted value and / or Diffusing capacity for carbon monoxide ((DLCO) <30% of predicted value or inability to achieve the Functional Respiratory Investigations (EFR) due to respiratory severity. EFR dated less than 3 months. Absence of argument for acute or subacute exacerbation in the last 6 months. Patient who can be followed in ambulatory consultation/ outpatient consultation. Informed consent signed (signed by the patient or in the presence of a third party for patients who are poorly fluent in French). Affiliation to the social security system. Exclusion Criteria: Patient unable to respond to quality of life questionnaires. Inability (physical or mental) to give a written informed consent. Acute exacerbation of fibrosis in the previous 6 months. Patient eligible for a pulmonary transplant. Participation in other therapeutic trial Patient cannot be followed in ambulatory consultation. Patient under trustee
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Boris Duchemann, Dr
Phone
01 48 95 50 32
Email
boris.duchemann@aphp.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Nacira DARGHAL, PhD
Phone
01 48 95 74 73
Email
nacira.darghal@aphp.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Boris Duchemann
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre Hospitalier Robert Ballanger
City
Aulnay-sous-Bois
ZIP/Postal Code
93602
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jérome VIRALLY, Pr
Facility Name
Hôpital Avicenne
City
Bobigny
ZIP/Postal Code
93000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Boris DUCHEMANN, PI
Facility Name
Centre Hospitalier de Versailles Andre Mignot
City
Le Chesnay
ZIP/Postal Code
78150
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nathalie MICHENOT, Dr
Facility Name
Hôpital LOUIS PRADEL
City
Lyon
ZIP/Postal Code
69677
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Vicent COTTIN, Pr
Facility Name
Hôpital NORD
City
Marseille
ZIP/Postal Code
13015
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Martine REYNAUD GAUBERT, Pr
Facility Name
Hôpital MARC JACQUET
City
Melun
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Djamel BENNEGADI, Dr
Facility Name
Hôpital GEORGES POMPIDOU (HEGP)
City
Paris
ZIP/Postal Code
75015
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dominique ISRAEL-BIET, Pr
Facility Name
Hôpital Tenon
City
Paris
ZIP/Postal Code
75020
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jean Marc NACCACHE, Pr
Facility Name
Hôpital Pontchaillou
City
Rennes
ZIP/Postal Code
35033
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stéphane JOUNEAU, Pr
Facility Name
Hôpital DELAFONTAINE
City
Saint-Denis
ZIP/Postal Code
93200
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Isabelle LERAT, Dr
Facility Name
Hôpital LARREY
City
Toulouse
ZIP/Postal Code
31059
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Grégoire PREVOT, Dr

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
19815403
Citation
Swigris JJ, Brown KK, Behr J, du Bois RM, King TE, Raghu G, Wamboldt FS. The SF-36 and SGRQ: validity and first look at minimum important differences in IPF. Respir Med. 2010 Feb;104(2):296-304. doi: 10.1016/j.rmed.2009.09.006. Epub 2009 Oct 7.
Results Reference
background
PubMed Identifier
15994268
Citation
Swigris JJ, Kuschner WG, Jacobs SS, Wilson SR, Gould MK. Health-related quality of life in patients with idiopathic pulmonary fibrosis: a systematic review. Thorax. 2005 Jul;60(7):588-94. doi: 10.1136/thx.2004.035220.
Results Reference
background
PubMed Identifier
20818875
Citation
Temel JS, Greer JA, Muzikansky A, Gallagher ER, Admane S, Jackson VA, Dahlin CM, Blinderman CD, Jacobsen J, Pirl WF, Billings JA, Lynch TJ. Early palliative care for patients with metastatic non-small-cell lung cancer. N Engl J Med. 2010 Aug 19;363(8):733-42. doi: 10.1056/NEJMoa1000678.
Results Reference
background

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Impact of a Systematic Palliative Care on Quality of Life, in Advanced Idiopathic Pulmonary Fibrosis.

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