Pain assessment and management deficiencies in nursing homes (NHs) are well documented. Unrelieved pain in this setting results in poorer resident outcomes, including depression, decreased mobility, sleep disturbance, and impaired physical and social functioning. This randomized controlled trial will evaluate the efficacy of a pain management algorithm coupled with intense diffusion strategies in improving pain, physical function and depression among NH residents. Specific aims of the study are to: 1) Evaluate the effectiveness of a pain management algorithm (ALG) coupled with intense diffusion strategies, as compared with pain education (EDU) and weak diffusion strategies, in improving pain, mobility, and depression among NH residents; 2) Determine the extent to which adherence to the ALG and organizational factors are associated with changes in resident outcomes and the extent to which changes in these variables are associated with changes in outcomes; 3) Evaluate the persistence of changes in process and outcome variables at long-term follow-up and 4) Evaluate the relationships among behavioral problems and pain in severely cognitively impaired residents who are unable to provide self-report.
Inadequate pain management in nursing homes (NHs) is well documented. Unrelieved pain in this setting results in depression, decreased mobility, sleep disturbance, and impaired physical and social functioning. This randomized controlled trial will evaluate the efficacy of a pain management algorithm delivered using intense diffusion strategies. Outcomes are facility pain practices and residents' pain, physical function and depression. Specific aims of the study are to: 1) Evaluate the effectiveness of a pain management algorithm (ALG) coupled with intense diffusion strategies, as compared with pain education (EDU) and weak diffusion strategies, in improving pain, mobility, and depression among NH residents; 2) Determine the extent to which adherence to the ALG and organizational factors are associated with changes in resident outcomes and the extent to which changes in these variables are associated with changes in outcomes; 3) Evaluate the persistence of changes in process and outcome variables at long-term follow-up and 4) Evaluate the relationships among behavioral problems and pain in severely cognitively impaired residents who are unable to provide self-report.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Enrollment
396
The NH pain management algorithm is a series of decision-making tools that begin with regular, comprehensive pain assessment matched to residents' cognitive status and proceed through analgesic therapy appropriate to the character, severity, and pattern of pain.
Swedish Medical Center
Seattle, Washington, United States
Change from Baseline in Pain at 3 months
Brief Pain Inventory (self-reporting participants) Nursing Assistant Surrogate Report
Time frame: 3 months
Change from Baseline in Pain at 6 months
Brief Pain Inventory (self-reporting participants) Nursing Assistant Surrogate Report
Time frame: 6 months post intervention
Change from Baseline in Mobility at 3 months
Functional independence measure - locomotion
Time frame: 3 months
Change from Baseline in Agitation at 6 months
Pittsburgh Agitation Scale
Time frame: 6 months
Change from Baseline Adherence to Best Practices at 3 months
Pain Management Chart audit Tool; 17 item tool evalauting staff adherence to recommended pain assessment and management practices
Time frame: 3 months
Change from Baseline in Depression at 3 months
Cornell Scale for Depression in Dementia
Time frame: 3 months
Change from Baseline in Depression at 6 months
Cornell Scale for Depression in Dementia
Time frame: 6 months post intervention
Change from Baseline in Mobility at 6 months
Functional independence measure - locomotion
Time frame: 6 months post-intervention
Change from Baseline in Adherence to Best Practices at 6 months
Pain Management Chart audit Tool; 17 item tool evalauting staff adherence to recommended pain assessment and management practices
Time frame: 6 months post-intervention
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