Improving Pain Management in Nursing Homes: A Research Project to Enhance Care Practices

NCT ID: NCT06984042

Last Updated: 2025-05-22

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

14 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-07-20

Study Completion Date

2024-11-20

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This study aims to improve the way pain is managed in nursing homes. It focuses on training staff, creating better systems to track pain, and involving residents and their families in decision-making. The goal is to provide better, more personalized care for residents, making sure their pain is properly managed and that the staff is well-equipped to support them.

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.

Pain Management Nursing Homes Elderly Pain Health Care Quality, Access, and Evaluation Patient-Centered Care

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

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

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

For residents:

* 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

For residents:

* 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
Minimum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Centre Hospitalier de Gonesse

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

France

Gonesse, , France

Site Status

Countries

Review the countries where the study has at least one active or historical site.

France

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

0084_GERIATRIE

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Cohort of Nursing Homes
NCT07249086 RECRUITING
Advanced Dementia and End-of-life
NCT03548142 COMPLETED NA