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Nursing Home Pain Management Algorithm Clinical Trial

Nursing Home Pain Management Algorithm Clinical Trial

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01399567
Enrollment
396
Registered
2011-07-22
Start date
2006-09-30
Completion date
2010-01-31
Last updated
2011-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain

Keywords

pain, depression, nursing homes, diffusion of innovations, clinical trial

Brief summary

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.

Detailed description

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.

Interventions

BEHAVIORALAlgorithm

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.

Sponsors

Swedish Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* long-term nursing home residents, * 65 years and older, * with moderate or greater pain in the week prior to screening, * residing in a participating facility, * who consent to participate (or whose surrogate decisionmaker consents to participation)

Exclusion criteria

* short-term stay patients, * persons less than 65 years, * residents on hospice

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline in Pain at 3 months3 monthsBrief Pain Inventory (self-reporting participants) Nursing Assistant Surrogate Report
Change from Baseline in Pain at 6 months6 months post interventionBrief Pain Inventory (self-reporting participants) Nursing Assistant Surrogate Report

Secondary

MeasureTime frameDescription
Change from Baseline Adherence to Best Practices at 3 months3 monthsPain Management Chart audit Tool; 17 item tool evalauting staff adherence to recommended pain assessment and management practices
Change from Baseline in Depression at 3 months3 monthsCornell Scale for Depression in Dementia
Change from Baseline in Agitation at 6 months6 monthsPittsburgh Agitation Scale
Change from Baseline in Mobility at 6 months6 months post-interventionFunctional independence measure - locomotion
Change from Baseline in Adherence to Best Practices at 6 months6 months post-interventionPain Management Chart audit Tool; 17 item tool evalauting staff adherence to recommended pain assessment and management practices
Change from Baseline in Depression at 6 months6 months post interventionCornell Scale for Depression in Dementia
Change from Baseline in Mobility at 3 months3 monthsFunctional independence measure - locomotion

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026