Assessment of the Burden Within the Dyad Patient/Caregiver
NCT ID: NCT00921232
Last Updated: 2012-07-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
139 participants
INTERVENTIONAL
2007-04-30
2008-02-29
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
This is a behavioral sciences study (= interventional study for french law)
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
CAREGIVER2, Caregiver's Health Assessment : Clinical and Biological Markers
NCT02521740
The Effectiveness of the Care Programme for the Last Days of Life
NCT01890239
Intervention Programs for Decreasing Caregiver Burden in Caregivers of Patients With Dementia
NCT02397980
Interventional Research With Mixed Methods on an Early Integrated Palliative Approach in Nursing Home
NCT04708002
Home-based Nurse Intervention in the Care of High Risk of Death Patients After Discharge From Geriatric Department
NCT06481917
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
dyad
life-ending patient and its caregiver
Questionnaires
During a consultation:
* 3 questionnaires (HADS, FRI, CRA)
* and a form for the sociodemographic data
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Questionnaires
During a consultation:
* 3 questionnaires (HADS, FRI, CRA)
* and a form for the sociodemographic data
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Cancer for which no curative treatment is envisaged
* Palliative treatment only
* For the caregiver: designated by the patient like the referring individual
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Unité de REcherche en sciences Cognitives et Affectives URECA EA1059
UNKNOWN
University of Lille Nord de France
OTHER
Centre Oscar Lambret
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Nicolas PENEL, MD
Role: PRINCIPAL_INVESTIGATOR
Centre Oscar Lambret
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Centre Oscar Lambret
Lille, , France
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
RAPSODIE
Identifier Type: -
Identifier Source: org_study_id
NCT00958594
Identifier Type: -
Identifier Source: nct_alias
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.