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

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02551965
Acronym
TANGO
Enrollment
200
Registered
2015-09-16
Start date
2016-01-31
Completion date
2023-09-30
Last updated
2020-07-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Exhaustion, Geriatric Disorder

Keywords

Cancer, Patient, Oncology, Caregiver

Brief summary

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

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

Interventions

OTHERPhone 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

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Standard collection of caregivers support frequency6 monthssubjects will be followed for the duration of patient treatment and follow-up in geriatric department, an average of 6 months. The caregivers support frequency will be reported during this period, depending on patient disease and caregiver tasks.
Standard collection of economic caregivers features6 monthssubjects will be followed for the duration of patient treatment and follow-up in geriatric department, an average of 6 months. The economic features will be reported during this period, depending on patient disease and caregiver tasks.
Standard collection of physical health caregivers features6 monthssubjects will be followed for the duration of patient treatment and follow-up in geriatric department, an average of 6 months. The physical health features will be reported during this period, depending on patient disease and caregiver tasks.
Standard collection of psychological health caregivers features6 monthssubjects will be followed for the duration of patient treatment and follow-up in geriatric department, an average of 6 months. The psychological health features will be reported during this period, depending on patient disease and caregiver tasks.
Standard collection of sociodemographic caregivers features6 monthssubjects will be followed for the duration of patient treatment and follow-up in geriatric department, an average of 6 months. The sociodemographic features will be reported during this period, depending on patient disease and caregiver tasks.

Secondary

MeasureTime frameDescription
The exhaustion level felt by caregiver is assessed with Mini-Zarit scale6 monthssubjects will be followed for the duration of patient treatment and follow-up in geriatric department, an average of 6 months
Medium delay of caregiver exhaustion apparition is assessed with Mini-Zarit scale6 monthsAn exhaustion is noticed when caregiver score is ≥ 2 on Mini-Zarit scale. However, the medium delay of caregiver exhaustion apparition is also assessed with an increasing of 2 points from caregiver baseline score on mini-Zarit scale. subjects will be followed for the duration of patient treatment and follow-up in geriatric department, an average of 6 months
Factors associated with medium delay of caregiver exhaustion apparition are determined with caregiver and patient features6 monthssubjects will be followed for the duration of patient treatment and follow-up in geriatric department, an average of 6 months

Countries

France

Contacts

Primary ContactAnne Laudamy
anne.laudamy@chru-strasbourg.fr+33 3 88 11 66 88
Backup Contactanatta Razafimanantsoa
anatta.razafimanantsoa@chru-strasbourg.fr+ 33 3 88 11 54 14

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026