search
Back to results

Dissemination of Injury Interventions

Primary Purpose

Fall Injury

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
facilitative system
Standard Program
Sponsored by
Medical College of Wisconsin
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Fall Injury focused on measuring Fall injury hospitalization, Fall injury emergency department visit, Fall injury death

Eligibility Criteria

65 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Communities interested in participating

Exclusion Criteria:

  • Existing facilitative system in community

Sites / Locations

  • Medical College of Wisconsin

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

No Intervention

Active Comparator

Experimental

Arm Label

Control

Standard Program

Facilitative System

Arm Description

a control group receiving no special resources or guidance related to fall injury prevention or the community health improvement process;

a "Standard Program" group receiving modest funding to implement an "evidence-based" fall prevention program in their local community;

a "Facilitative System" group receiving facilitative system support in addition to the resources provided the Standard Program group

Outcomes

Primary Outcome Measures

Emergency Department and In-patient Hospitalization for Fall Injury
Rates of fall injury diagnoses per 100 person-years (P-Y) were computed for the communities in each of the study groups for a 2 year baseline period, 2007-2008, and for a 2 year follow-up period corresponding to years 2010-2011. Change in fall injury rates and their 95% confidence intervals (CI) are reported. A mixed-effects Poisson regression model was used to test the presence of an interaction effect on the fall rate between study group and time period (baseline or follow-up). The test is intended to detect a differential time effect by study group. This model, with main effects for study group and time period and an interaction term, will be referred to as the primary model. Model coefficients and incidence rate ratios (IRR) with 95% confidence intervals (CI) are reported.

Secondary Outcome Measures

Full Information

First Posted
July 31, 2008
Last Updated
February 3, 2015
Sponsor
Medical College of Wisconsin
search

1. Study Identification

Unique Protocol Identification Number
NCT00729521
Brief Title
Dissemination of Injury Interventions
Official Title
Facilitating Dissemination of Injury Interventions: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2015
Overall Recruitment Status
Completed
Study Start Date
July 2007 (undefined)
Primary Completion Date
July 2012 (Actual)
Study Completion Date
July 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical College of Wisconsin

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
An important challenge for the field of injury prevention and control is the translation of research findings into effective community-based prevention programs and practices. The National Center for Injury Prevention and Control believes that dissemination research can overcome this challenge by providing insight into the structures and methods needed to translate injury control research into everyday practice. The proposed dissemination research study will rigorously assess whether the use of a "facilitative system" can successfully bridge the gap between injury prevention and control research and the implementation of evidence-driven, community-based programs, policies, and practices. The facilitative system links communities with academic partners to provide communities with the skills and resources needed to help facilitate the community health improvement process. The system identifies what assets are available within communities, as well as the skills and resources needed to work through the community health improvement process. The facilitative system will then provide technical assistance, best practices guides, and direct consultation in carrying out all phases of the community health improvement process. This information is designed to increase community capacity in community assessment, coalition development, accessing and interpreting local injury prevention data, searching and selecting evidence-based research, and program planning and evaluation. The study will use a randomized community trial design to evaluate fall injury occurrence and process measures of program implementation in three groups of communities: a control group receiving no special resources or guidance related to fall injury prevention or the community health improvement process; a "Standard Program" group receiving modest funding to implement an "evidence-based" fall prevention program in their local community; a "Facilitative System" group receiving facilitative system support in addition to the resources provided the Standard Program group. We hypothesize that the Facilitative System program will be more effective at: reducing fall-related injuries in the elderly; building community coalitions that are goal-oriented and sustainable; implementing community-based, evidence-driven fall prevention programs that are both tailored to the community needs and yet faithful to empirically-tested fall prevention research studies

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fall Injury
Keywords
Fall injury hospitalization, Fall injury emergency department visit, Fall injury death

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
35037 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Description
a control group receiving no special resources or guidance related to fall injury prevention or the community health improvement process;
Arm Title
Standard Program
Arm Type
Active Comparator
Arm Description
a "Standard Program" group receiving modest funding to implement an "evidence-based" fall prevention program in their local community;
Arm Title
Facilitative System
Arm Type
Experimental
Arm Description
a "Facilitative System" group receiving facilitative system support in addition to the resources provided the Standard Program group
Intervention Type
Other
Intervention Name(s)
facilitative system
Intervention Description
The facilitative system links communities with academic partners to provide communities with the skills and resources needed to help facilitate the community health improvement process. The system identifies what assets are available within communities, as well as the skills and resources needed to work through the community health improvement process. The facilitative system will then provide technical assistance, best practices guides, and direct consultation in carrying out all phases of the community health improvement process. This information is designed to increase community capacity in community assessment, coalition development, accessing and interpreting local injury prevention data, searching and selecting evidence-based research, and program planning and evaluation.
Intervention Type
Other
Intervention Name(s)
Standard Program
Intervention Description
a "Standard Program" group receiving modest funding to implement an "evidence-based" fall prevention program in their local community;
Primary Outcome Measure Information:
Title
Emergency Department and In-patient Hospitalization for Fall Injury
Description
Rates of fall injury diagnoses per 100 person-years (P-Y) were computed for the communities in each of the study groups for a 2 year baseline period, 2007-2008, and for a 2 year follow-up period corresponding to years 2010-2011. Change in fall injury rates and their 95% confidence intervals (CI) are reported. A mixed-effects Poisson regression model was used to test the presence of an interaction effect on the fall rate between study group and time period (baseline or follow-up). The test is intended to detect a differential time effect by study group. This model, with main effects for study group and time period and an interaction term, will be referred to as the primary model. Model coefficients and incidence rate ratios (IRR) with 95% confidence intervals (CI) are reported.
Time Frame
2007-2008; 2010-2011

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Communities interested in participating Exclusion Criteria: Existing facilitative system in community
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter M Layde, MD
Organizational Affiliation
Medical College of Wisconsin
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medical College of Wisconsin
City
Milwaukee
State/Province
Wisconsin
ZIP/Postal Code
53226
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Dissemination of Injury Interventions

We'll reach out to this number within 24 hrs