Actively Recruiting
Testing the Pain Clinical Practice Guideline
Led by University of Maryland, Baltimore · Updated on 2026-05-08
300
Participants Needed
11
Research Sites
265 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
There are evidence based processes for assessment and management of pain using pharmacologic and nonpharmacological approaches. These were reviewed and included within the Pain Management Clinical Practice Guideline (Pain Management CPG) recently developed by AMDA: The Society for Post-Acute and Long-Term Care Medicine. There are, however, many challenges to translating the use of Clinical Practice Guidelines into clinical settings. To overcome these challenges we developed and previously tested a theoretically based approach and merged this approach with the Pain Management CPG, which is referred to as the PAIN-CLINICAL PRACTICE GUIDELINE-USING THE EVIDENCE INTEGRATION TRIANGLE (PAIN-CPG-EIT). The PAIN-CPG-EIT involves a research nurse facilitator working with an identified community champion(s) and stakeholder team for 12 months to provide the following four components: Component I: Establishing and meeting monthly with a Stakeholder Team; Component II: Education of the staff; Component III: Mentoring and motivating the staff to address pain; Component IV: Ongoing evaluation of resident pain outcomes. Twelve communities will be included with 25 residents living with dementia and pain recruited from each community. Six communities will be randomized to treatment (PAIN-CPG-EIT) and six randomized to education only (EO) which involves providing the same education to staff as is done in Component II of PAIN-CPG-EIT. The primary aim of this study is to test the effectiveness of use of the PAIN-CPG-EIT to improve the assessment, diagnosis and management of pain and decrease pain intensity among nursing home residents living with dementia between baseline, 4 and 12 months and evaluate treatment fidelity. A secondary aim of the study is to consider differences in measurement, treatment and response to treatment between male and female and Black versus White residents living with dementia. Findings from this study will help build on the currently limited information about pain presentation and management among older adults living with dementia in nursing homes and improve health equity of aging populations experiencing pain.
CONDITIONS
Official Title
Testing the Pain Clinical Practice Guideline
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Living in a participating community
- 60 years of age or older
- Evidence of dementia based on scores from BIMS, AD8, Clinical Dementia Rating Scale, and Functional Activities Questionnaire
- Evidence of pain at recruitment, including experiencing pain occasionally, frequently, or almost constantly over the past 5 days, staff report of pain, or current pain treatment
You will not qualify if you...
- Admitted to the nursing home for short-stay rehabilitation or other subacute needs such as intravenous antibiotics
- Receiving hospice care
AI-Screening
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Trial Site Locations
Total: 11 locations
1
Future Care Coldspring
Baltimore, Maryland, United States, 21218-1708
Completed
2
Future Care Courtland
Baltimore, Maryland, United States, 21218-1708
Active, Not Recruiting
3
Futurecare Northpoint
Baltimore, Maryland, United States, 21224
Active, Not Recruiting
4
Futurecare Irvington
Baltimore, Maryland, United States, 21229
Active, Not Recruiting
5
Lorein Bel Aire
Bel Air, Maryland, United States, 21015
Not Yet Recruiting
6
Lorien Columbia
Columbia, Maryland, United States, 21045
Not Yet Recruiting
7
Communicare Ellicott City
Ellicott City, Maryland, United States, 21042
Completed
8
communicare Marley Station
Glen Burnie, Maryland, United States, 21060
Completed
9
Lorien Bulle Rock
Havre de Grace, Maryland, United States, 21078
Actively Recruiting
10
Charles E Smilth Life Community
Rockville, Maryland, United States, 20852
Completed
11
Lorien Mays Chapel
Timonium, Maryland, United States, 21093
Not Yet Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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