Improving Pain Management in Nursing Homes: A Research Project to Enhance Care Practices
NCT ID: NCT06984042
Last Updated: 2025-05-22
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
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COMPLETED
14 participants
OBSERVATIONAL
2024-07-20
2024-11-20
Brief Summary
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Detailed Description
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Conditions
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Study Design
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OTHER
PROSPECTIVE
Study Groups
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Residents of EHPAD
2 residents
No interventions assigned to this group
Family or close
2 family members or close
No interventions assigned to this group
Healthcare professionals
1 psychologist, 1 head of department, 1 health manager, 2 IDE, 2 AS, 2 AVS and 1 quality engineer.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Aged 60 years or older
* Living in the nursing home (EHPAD) for at least 3 months
* Presence of chronic or acute pain requiring regular management
* Willing to participate in a semi-structured interview
* Provided informed and signed consent to participate in the study
For family members or close relatives:
* Family member or close relative who visits the resident regularly
* Actively involved in the resident's care or support
* Willing to participate in a semi-structured interview
* Provided informed consent to participate in the study
For healthcare professionals:
* Registered nurses (RN), nursing assistants (NA), or support staff (AVS) involved in professional practice analysis groups
* Nurse managers, department heads, psychologists of the nursing home, or the hospital's quality engineer participating in semi-structured interviews
* Voluntary participation with informed and signed consent
* Available to participate in all stages of the project
Exclusion Criteria
* Under 60 years of age
* Living in the nursing home for less than 3 months
* Absence of pain requiring regular management
* Cognitive impairment preventing participation in interviews
* Refusal or inability to participate in discussion and exchange sessions
* Unwillingness to take part in a semi-structured interview
* Inability to provide informed and signed consent
* Resident in end-of-life care
For family members or close relatives:
* Family member or relative with infrequent contact with the resident
* Refusal or inability to participate in discussion and exchange sessions
* Refusal to sign informed consent for participation
* Unwillingness to take part in a semi-structured interview
For healthcare professionals:
* Refusal or inability to participate in group discussions or semi-structured interviews
* Refusal to sign informed consent for participation
* Temporary, freelance, or external professionals not part of the regular care team
* Professionals mandated or forced to participate in practice analysis groups
* Unavailable to participate in all stages of the project
60 Years
ALL
No
Sponsors
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Centre Hospitalier de Gonesse
OTHER
Responsible Party
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Locations
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France
Gonesse, , France
Countries
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Other Identifiers
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0084_GERIATRIE
Identifier Type: -
Identifier Source: org_study_id
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