Pain, Acute Clinical Trial
Official title:
Improving PAIN Control Following FRactures; Towards an Elder-friendly Emergency Department
The PAINFREE (Improving PAIN control following FRactures; towards an Elder-friendly Emergency
department) Initiative is a patient-centered multifaceted intervention which aims to improve
pain management in patients 75 years and older presenting with a fracture at 7 Emergency
Department of participating Montreal hospitals:
1. Montreal General Hospital
2. Royal Victoria Hospital
3. Ste Mary's Hospital
4. Hôpital de Verdun
5. Hôpital du Sacré-Coeur de Montréal
6. Jewish General Hospital
7. Lakeshore General Hospital
Using a stepped-wedge cluster randomized trial design, we will implement PAINFREE
sequentially in 7 Emergency Departments (EDs) in the greater Montreal area where as each ED
site acts as its own control and provides data in both pre- and post-implementation periods.
Mixed methods analysis will be used to link quantitative (pain management indicators pre- and
post-implementation) to qualitative (feasibility, fidelity and acceptability of
implementation) data sets to facilitate data triangulation to evaluate the effects of
PAINFREE in real world settings.
PAINFREE Initiative at each site includes 3 phases: pre-implementation, implementation, and
post-implementation. The approach is patient-centered and is composed of three complementary
components: a patient component, a physician component, and a nursing component.
Each program phases include the following steps:
1. Pre-implementation (2 months):
1. In all study sites, distribution and analysis of a web-based survey for nurses to
document factors that can impact PAINFREE implementation in their environment
2. Review of medical records of the target population for extraction of selected
variables
2. PAINFREE implementation (6 months):
1. Awareness campaigns will be organized throughout the institution of each study site
(posters, brochures, billboards, lanyards)
2. Profession-specific educational presentations (1 hour) for physicians and nurses,
accredited as part of continued professional development programs
3. Distribution of standardized point-of-care tools to improve pain assessment and
documentation (pocket cards, use of validated pain scales), treatment (standardized
prescription) and re-assessment
4. Distribution of educational material and tools targeting pain care literacy (pain
scale interpretation, pamphlet) for patients and their families
3. Post-implementation (4 months):
1. Review of medical records of target population for extraction of selected variables
2. Distribution of report cards comparing each ED's post- and pre-intervention
performance on pain management indicators and comparing their performance to that
of other sites
3. Phone call interviews with patients
4. Focus group interviews (physicians and nurses)
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05396820 -
Adaptation of the Motor System to Experimental Pain
|
N/A | |
Completed |
NCT04356963 -
Adjunct VR Pain Management in Acute Brain Injury
|
N/A | |
Recruiting |
NCT06350084 -
Effect of Mother's Touch and Nurse's Therapeutic Touch on Pain Level and Crying Time During Heel Blood Collection
|
N/A | |
Completed |
NCT04080037 -
Assessing Opioid Care Practices Using CPV Patient Simulation Modules
|
N/A | |
Recruiting |
NCT05458037 -
RCT of Pain Perception With Fast and Slow Tenaculum Application
|
N/A | |
Completed |
NCT04571515 -
Dose-Response Study of MR-107A-01 in The Treatment of Post-Surgical Dental Pain
|
Phase 2 | |
Completed |
NCT06005480 -
Understanding Rebound Pain After Regional Anesthesia Resolution in Healthy Volunteers
|
Phase 1 | |
Active, not recruiting |
NCT04850079 -
EHR Precision Drug Treatment in Neonates
|
||
Completed |
NCT03272139 -
Interscalene Block Versus Superior Trunk Block
|
Phase 4 | |
Completed |
NCT03271151 -
Effect of Duloxetine on Opioid Use After Total Knee Arthroplasty
|
Phase 4 | |
Recruiting |
NCT05383820 -
Effect of Paracetamol and Ketorolac on RANK-L Levels in Patients Starting Orthodontic Treatment
|
Phase 4 | |
Completed |
NCT04851353 -
Multiple Sensory Interventions On Infants' Pain and Physiological Distress During Neonatal Screening Procedures
|
N/A | |
Completed |
NCT03280017 -
Ketamine With Multilevel Paravertebral Block for Post Video-assisted Thoracic Surgery Pain
|
Phase 4 | |
Completed |
NCT04280796 -
Changes in Affective Pain Processing in Human Volunteers
|
N/A | |
Not yet recruiting |
NCT04491630 -
COping With PAin Through Hypnosis, Mindfulness and Spirituality
|
N/A | |
Not yet recruiting |
NCT04523623 -
Pain Control Differences Between Oxycodone and Ibuprofen in Children With Isolated Forearm Injuries
|
N/A | |
Not yet recruiting |
NCT04062513 -
Olfactive Stimulation Interventions With Mothers' Milk on Preterm Pain Response
|
N/A | |
Withdrawn |
NCT03137017 -
A Comparison of Plasma Concentrations of Hydrocodone and Acetaminophen After Administration of a New and a Marketed Tablet Formulation Under Fasted and Fed Conditions in Healthy Adults
|
Phase 1 | |
Withdrawn |
NCT03137030 -
A Comparison of Plasma Concentrations of Hydrocodone and Acetaminophen After Administration of Different Amounts of Tablets of a New and a Marketed Tablet Formulation in Healthy Adults
|
Phase 1 | |
Completed |
NCT04659395 -
How to Develop a Training Program for Nurses in Ultrasound Guided Femoral Nerve Block
|
N/A |