Nursing Follow up in Geriatric Oncology : Tracking Time of Caregiver Exhaustion Risk

NCT ID: NCT02551965

Last Updated: 2020-07-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

200 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-01-31

Study Completion Date

2023-09-30

Brief Summary

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In geriatric oncology, caregivers are submitted to a risk of exhaustion. To investigate the clinical risk factor of exhaustion, the researchers propose to conduct a prospective observational study during 6 months phone follow up of the caregivers. The recruitment will take place during the oncogeriatric assessment consultation.

Detailed Description

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The primary purpose aim to describe the caregiver of patient with 70 years old or more, suffered from cancer and for which a treatment is planned, along with their long term evolution.

The secondary purposes are to :

* Assess the exhaustion level felt by this caregiver
* Assess the medium delay of caregiver exhaustion apparition
* Relate factors associated to the medium delay of caregiver exhaustion apparition during patient chemotherapy and/or radiotherapy treatment

Conditions

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Exhaustion Geriatric Disorder

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Caregiver of cancer patient followed in geriatric oncology

caregiver of cancer patient with 70 years old or more, for which a treatment is planned, along with their long term evolution

Group Type EXPERIMENTAL

Phone nursing follow-up

Intervention Type OTHER

From the day of geriatric cancer patient's consultation, nurses will identify caregiver and will follow them by phone (caregiver) during 6 months

Interventions

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Phone nursing follow-up

From the day of geriatric cancer patient's consultation, nurses will identify caregiver and will follow them by phone (caregiver) during 6 months

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Caregiver of :

* patient with 70 years old or more, suffered from cancer and receiving specific cancer treatment (chemotherapy or radiotherapy )
* Patient evaluated in a specific comprehensive oncogeriatric assessment
* informed patient given a non-opposition form
* Patient affiliated to a social protection scheme
* Informed consent given by the caregiver

Exclusion Criteria

* Patient and caregiver under judicial protection
* Caregiver with understanding difficulties with French language
* Psychological, familial, social or geographic conditions that avoid a good clinical trial continuity
* Patient with ≤ 18 years old
* Caregiver and patient with significant cognitive troubles
* Caregiver and patient located in institution during inclusion period
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University Hospital, Strasbourg, France

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Damien HEITZ, MD

Role: PRINCIPAL_INVESTIGATOR

Strasbourg's University Hospitals - UCROG

Locations

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Unité de Coordination Régionale en Oncogériatrie - Hôpital de Hautepierre

Strasbourg, , France

Site Status RECRUITING

Countries

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France

Central Contacts

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Anne Laudamy

Role: CONTACT

+33 3 88 11 66 88

anatta Razafimanantsoa

Role: CONTACT

+ 33 3 88 11 54 14

Facility Contacts

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Damien HEITZ, PH

Role: primary

03 88 12 86 57

Gwenaelle BOSSU

Role: backup

03 88 12 86 57

Other Identifiers

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6116

Identifier Type: -

Identifier Source: org_study_id

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