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Assessment and Prevention of Caregiver Burden in Oncology (PREPAC-01)

Primary Purpose

Oncology, Caregiver Burden

Status
Not yet recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Specific nursing support
Non-specific nursing support
Sponsored by
Institut Cancerologie de l'Ouest
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Oncology focused on measuring Nurse, Supportive Care, Zarit scale, Caregiver Burden

Eligibility Criteria

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

Inclusion Criteria: Caregiver designated by the patient; Caregiver of a patient who started a line (any line) of systemic treatment for a solid tumour since less than 3 months or in an active palliative situation since less than 1 month; Caregiver of patient already cared for by a nurse before inclusion or going to start a nursing follow-up; Caregiver of a patient with a score ≥2 of social fragility and/or psychological fragility and/or nutritional fragility and/or complexity; Exclusion Criteria: Patient whose life expectancy is assumed to be < 6 months; Patient living in an institution (EHPAD, MAS, SSR, MCO, USLD) at inclusion; Caregiver declared as having a pathology that could alter his/her capacity to support (psychiatric history, dementia…) or under guardianship.

Sites / Locations

  • CH Cholet
  • Centre Antoine Lacassagne
  • Centre Henri Bequerel
  • Institut de Cancérologie de l'Ouest
  • CH Mémorial de Saint Lo

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Specific nursing support

No specific nursing support

Arm Description

The caregivers benefit from specific nursing support.

Caregivers do not receive any specific support from the nurses.

Outcomes

Primary Outcome Measures

Caregiver burden
Comparison in the 2 groups. Burden score is assessed using the ZARIT SCALE. The test consists of 22 questions that the caregiver has to score from 0 to 4, the whole giving a score from 0 to 88. 0 means no burden, 88 means that the burden is severe

Secondary Outcome Measures

The level of anxiety/depression of the caregiver
Comparaison in the 2 groups. Hospital Anxiety and Depression scale consists of 14 items to which participants respond on a 4-point Likert scale. Seven items assess anxiety and seven items assess depression. Anxiety and depression scores can range from 0 (no symptoms) to 21 (significant presence of symptoms). Threshold scores were determined as follows: between 0 and 7 : no symptoms of anxiety or depression; between 8 and 10 : some moderate symptoms (mild anxiety or depression); score of 11 or more : significant number of symptoms (severe anxiety or depression).
Caregiver's quality of life
Comparison in the 2 groups. The generic self-questionnaire SF36 consists of 36 items concerning the last four weeks before the test and divided into 8 dimensions (Physical activity ; Life and relationships with others ; Physical pain; Perceived health ; Vitality; Limitations due to the psychological state; Limitations due to the physical state; Psychological health). These eight dimensions are used to measure two summary scores of the quality of life of individuals: the physical composite score (PCS) and the mental composite score (MCS). (score from 0 to 100). A low score reflects a perception of poor health, loss of function, presence of pain. A high score reflects a perception of good health, absence of functional deficit and pain.
Caregiver's satisfaction
Only arm B. P-GIC questionnaire consists of a single question asking the caregiver about their overall impression of change in specific support care. The caregiver is given the following 8 options and asked to indicate which of these best describes the perceived change: I don't know, Very strongly positive, Strongly positive, Slightly positive, No change, Slightly negative, Strongly negative, Very strongly negative.

Full Information

First Posted
February 20, 2023
Last Updated
June 26, 2023
Sponsor
Institut Cancerologie de l'Ouest
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1. Study Identification

Unique Protocol Identification Number
NCT05750836
Brief Title
Assessment and Prevention of Caregiver Burden in Oncology
Acronym
PREPAC-01
Official Title
Assessment and Prevention of Caregiver Burden in Oncology
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
July 2023 (Anticipated)
Primary Completion Date
January 2027 (Anticipated)
Study Completion Date
June 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institut Cancerologie de l'Ouest

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
The goal of this randomized, open and controlled supportive care study is to see if we can reduce the burden on the caregiver by offering the caregiver systematic and regular support from the nurse (APN, nurse coordinator in French health care organisations) compared to a support focused on the patient. At the same time, we will also evaluate the impact of this personalised support for the caregiver on their anxiety and quality of life. Participants will caregivers of a patient who started a line (any line) of systemic treatment for a solid tumour since less than 3 months or in an active palliative situation since less than 1 month. Researchers will compare 2 groups : a group where caregivers benefit from specific nursing support and a group of caregivers with no specific nursing support. The specific support includes 3 mandatory on-site nursing consultations with the patient's caregiver and interviews once a month with a nurse either by phone, on-site consultation or teleconsultation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Oncology, Caregiver Burden
Keywords
Nurse, Supportive Care, Zarit scale, Caregiver Burden

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
250 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Specific nursing support
Arm Type
Experimental
Arm Description
The caregivers benefit from specific nursing support.
Arm Title
No specific nursing support
Arm Type
Active Comparator
Arm Description
Caregivers do not receive any specific support from the nurses.
Intervention Type
Other
Intervention Name(s)
Specific nursing support
Intervention Description
3 mandatory on-site nursing consultations with the patient's caregiver at inclusion, 6 months and 12 months post-randomisation.The caregivers will complete the questionnaires (Zarit scale, Hospital Anxiety and Depression scale, Medical Outcome Study Short Form - 36, Caregiver's satisfaction). interviews once a month with a nurse either by phone, on-site consultation or teleconsultation. Nurses assess the general health of the caregiver and Identify the socio-professional situation of the caregiver
Intervention Type
Other
Intervention Name(s)
Non-specific nursing support
Intervention Description
Caregivers will only have to complete on site Health indicators, Zarit scale, Hospital Anxiety and Depression scale, Medical Outcome Study Short Form - 36 at inclusion, 6 months and 12 months post-randomisation.
Primary Outcome Measure Information:
Title
Caregiver burden
Description
Comparison in the 2 groups. Burden score is assessed using the ZARIT SCALE. The test consists of 22 questions that the caregiver has to score from 0 to 4, the whole giving a score from 0 to 88. 0 means no burden, 88 means that the burden is severe
Time Frame
at 6 months post-randomisation
Secondary Outcome Measure Information:
Title
The level of anxiety/depression of the caregiver
Description
Comparaison in the 2 groups. Hospital Anxiety and Depression scale consists of 14 items to which participants respond on a 4-point Likert scale. Seven items assess anxiety and seven items assess depression. Anxiety and depression scores can range from 0 (no symptoms) to 21 (significant presence of symptoms). Threshold scores were determined as follows: between 0 and 7 : no symptoms of anxiety or depression; between 8 and 10 : some moderate symptoms (mild anxiety or depression); score of 11 or more : significant number of symptoms (severe anxiety or depression).
Time Frame
at month 6 (M6) and month 12 (M12) post-randomisation.
Title
Caregiver's quality of life
Description
Comparison in the 2 groups. The generic self-questionnaire SF36 consists of 36 items concerning the last four weeks before the test and divided into 8 dimensions (Physical activity ; Life and relationships with others ; Physical pain; Perceived health ; Vitality; Limitations due to the psychological state; Limitations due to the physical state; Psychological health). These eight dimensions are used to measure two summary scores of the quality of life of individuals: the physical composite score (PCS) and the mental composite score (MCS). (score from 0 to 100). A low score reflects a perception of poor health, loss of function, presence of pain. A high score reflects a perception of good health, absence of functional deficit and pain.
Time Frame
at month 6 (M6) and month 12 (M12) post-randomisation.
Title
Caregiver's satisfaction
Description
Only arm B. P-GIC questionnaire consists of a single question asking the caregiver about their overall impression of change in specific support care. The caregiver is given the following 8 options and asked to indicate which of these best describes the perceived change: I don't know, Very strongly positive, Strongly positive, Slightly positive, No change, Slightly negative, Strongly negative, Very strongly negative.
Time Frame
at month 6 (M6) and month 12 (M12) post-randomisation.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Caregiver designated by the patient; Caregiver of a patient who started a line (any line) of systemic treatment for a solid tumour since less than 3 months or in an active palliative situation since less than 1 month; Caregiver of patient already cared for by a nurse before inclusion or going to start a nursing follow-up; Caregiver of a patient with a score ≥2 of social fragility and/or psychological fragility and/or nutritional fragility and/or complexity; Exclusion Criteria: Patient whose life expectancy is assumed to be < 6 months; Patient living in an institution (EHPAD, MAS, SSR, MCO, USLD) at inclusion; Caregiver declared as having a pathology that could alter his/her capacity to support (psychiatric history, dementia…) or under guardianship.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Céline THOMAS, Nurse
Phone
(0)2 40 67 97 49
Ext
+33
Email
celine.thomas@ico.unicancer.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Emilie DEBEAUPUIS
Phone
(0)240679844
Ext
+33
Email
emilie.debeaupuis@ico.unicancer.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Céline THOMAS, Nurse
Organizational Affiliation
Institut de Cancérologie de l'Ouest
Official's Role
Principal Investigator
Facility Information:
Facility Name
CH Cholet
City
Cholet
ZIP/Postal Code
49300
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Margot NOBLECOURT, MD
Email
margot.noblecourt@ch-cholet.fr
Facility Name
Centre Antoine Lacassagne
City
Nice
ZIP/Postal Code
06 189
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
julie OUDIN, Nurse
Email
Julie.oudin@nice.unicancer.fr
Facility Name
Centre Henri Bequerel
City
Rouen
ZIP/Postal Code
76038
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Amel CONSTANTIN, Nurse
Email
amel.benchemam@chb.unicancer.fr
Facility Name
Institut de Cancérologie de l'Ouest
City
Saint Herblain
ZIP/Postal Code
44805
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Céline THOMAS, Nurse
Email
celine.thomas@ico.unicancer.fr
Facility Name
CH Mémorial de Saint Lo
City
Saint Lo
ZIP/Postal Code
50000
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Emillie LEFEVRE, Nurse
Email
emilie.lefevre@ch-stlo.fr

12. IPD Sharing Statement

Learn more about this trial

Assessment and Prevention of Caregiver Burden in Oncology

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