search
Back to results

Strategies to Reduce Injuries and Develop Confidence in Elders (STRIDE)

Primary Purpose

Accidental Falls, Wounds and Injuries

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Evidence-based tailored fall prevention
Usual care
Sponsored by
Brigham and Women's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Accidental Falls

Eligibility Criteria

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

Inclusion Criteria:

  • The patient is at least 70 years of age.
  • The patient must answer 'yes' to one or more of the following questions:
  • Have you fallen and hurt yourself in the past year?
  • Have you fallen 2 or more times in the past year?
  • Are you afraid that you might fall because of balance or walking problems?

Exclusion Criteria:

  • The patient is enrolled in hospice.
  • The patient resides in a nursing home.
  • The patient is not capable of providing informed consent (or assent), and a proxy is not available.
  • The patient does not speak English or Spanish

Sites / Locations

  • Healthcare Partners
  • University of Iowa Health Alliance
  • Johns Hopkins Medicine
  • Partners Healthcare
  • Reliant Medical Group
  • University of Michigan
  • Essentia Health
  • Mt Sinai Health System
  • University of Pittsburgh
  • University of Texas Medical Branch at Galveston

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Fall prevention standard of care

Control

Arm Description

An evidence-based patient-centered intervention that will combine elements of a multifactorial, risk factor-based, standardly-tailored fall prevention strategy developed at Yale, practice guidelines offered by the CDC's "STEADI" toolbox and the joint American Geriatrics Society/British Geriatrics Society guidelines, and ACOVE practice change approach

Usual fall prevention care

Outcomes

Primary Outcome Measures

First Adjudicated Serious Fall-Related Injury
Number of first adjudicated serious fall-related injury serious fall-related injury events per 100 per years of follow-up.

Secondary Outcome Measures

First Self-reported Fall-related Injury
Number of first self-reported fall-related injuries per 100 per years of follow-up
Time to Self-reported Falls
** data for this outcome was not collected
Physical Function
Late Life Function and Disability Instrument (LL-FDI) function score. The scores are on a 0-100 scale, higher score = better function. The measure reported is the mean of scores at the 12-month and 24-months follow-up assessment
Disability
Late Life Function and Disability Instrument (LL-FDI) disability score. The scores are on a 0-100 scale, higher score = less disability. The measure reported is the mean of scores at the 12-month and 24-months follow-up assessment
Anxiety
Patient-reported Outcome Measure Information System (PROMIS) Anxiety subscale. Measured on a 8-40 Scale, higher score = more anxiety.
Depression
PROMIS depression subscale. Measured on a 8-40 Scale, higher score = more depression.
Fear of Falling
Falls Efficacy Scale. Measured on a 10-40 Scale, higher score = more fear of falling.

Full Information

First Posted
June 1, 2015
Last Updated
March 2, 2021
Sponsor
Brigham and Women's Hospital
Collaborators
Yale University, University of California, Los Angeles, Healthcare Partners, The University of Texas Medical Branch, Galveston, University of Pittsburgh Medical Center, Johns Hopkins University, Mt Sinai Health System, Reliant Medical Group, Partners HealthCare, University of Michigan, University of Iowa Health Alliance, Essentia Health, Wake Forest University, National Institute on Aging (NIA), Patient-Centered Outcomes Research Institute, National Institutes of Health (NIH)
search

1. Study Identification

Unique Protocol Identification Number
NCT02475850
Brief Title
Strategies to Reduce Injuries and Develop Confidence in Elders
Acronym
STRIDE
Official Title
Randomized Trial of a Multifactorial Fall Injury Prevention Strategy
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
August 2015 (Actual)
Primary Completion Date
December 2019 (Actual)
Study Completion Date
January 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Brigham and Women's Hospital
Collaborators
Yale University, University of California, Los Angeles, Healthcare Partners, The University of Texas Medical Branch, Galveston, University of Pittsburgh Medical Center, Johns Hopkins University, Mt Sinai Health System, Reliant Medical Group, Partners HealthCare, University of Michigan, University of Iowa Health Alliance, Essentia Health, Wake Forest University, National Institute on Aging (NIA), Patient-Centered Outcomes Research Institute, National Institutes of Health (NIH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of this pragmatic cluster-randomized trial is to determine the effectiveness of an evidence-based, patient-centered multifactorial fall injury prevention strategy in community dwelling older adults at risk of falls recruited from 86 primary care practices around the U.S.
Detailed Description
Objective: To determine the effectiveness of an evidence-based, patient-centered multifactorial fall injury prevention strategy implemented within primary care practices using usual health care resources Design: This study is a cluster randomized, parallel group superiority trial with practices stratified by healthcare system and patients nested within practices. The unit of randomization is the practice. Study Duration: The total study duration is 5 years. Recruitment will take place over 20 months, with follow-up taking place for 24 months - 44 months depending on date of enrollment. Trial Sites: 86 primary care practices that are part of 10 trial sites located around the U.S.: The Partners' Health Care System; Essentia; Hopkins Health Care System; HealthCare Partners; Reliant Health Care System; Mount Sinai Health Care System; University of Pittsburgh Health Care System; University of Texas Medical Branch Health Care System; University of Iowa Health Care System; University of Michigan Health Care System. Number of Subjects: The original target sample size was 6,000 participants enrolled in 86 practices to provide 90% power to detect a 20% reduction in the rate of the primary outcome with intervention relative to control. The study was originally designed for a study duration of 36 months with 18 months of recruitment and a minimum of 18 months of follow-up. The study was extended to a 44 month study (20 months of recruitment and a minimum 24 month of follow-up). For a 44 month trial, it was estimated that a sample size of 5,322 subjects would provide 90% power to detect a 20% reduction in the rate of the primary outcome with the intervention relative to control. Main Inclusion Criteria Community-living persons, 70 years or older, who are at increased risk for serious fall injuries. Intervention: An evidence-based patient-centered intervention that will combine elements of a multifactorial, risk factor-based, standardly-tailored fall prevention strategy developed at Yale, practice guidelines offered by the Center for Disease Control's (CDC's) "STEADI" toolbox (Stopping Elderly Accidents, Disability and Injury) and the joint American Geriatrics Society/British Geriatrics Society guidelines, and Assessing Care of Vulnerable Elders (ACOVE) practice change approach. The fall prevention strategies will be systematically implemented into clinical practice using: delivery system design to improve quality (Co-management); decision support (algorithms); information systems (software); self-management support (patient/caregiver engagement and activation); and linkage to community-based resources. Primary Outcome: The primary outcome is adjudicated serious fall injuries, operationalized as a fall resulting in: (1) (fracture other than thoracic/lumbar vertebral; joint dislocation; or cut requiring closure) AND any medical attention; OR (2) (head injury; sprain or strain; bruising or swelling; or other) requiring hospitalization. Primary Analysis: The risk of any serious fall injury (i.e., time to first event) will be analyzed using a survival model that incorporates competing risks (due to death) and clustering. In this analysis, participants who are lost to follow-up without a prior serious fall-related injury will be censored at their date last seen. In a sensitivity analysis, the investigators will adjust for the pre-specified set of baseline covariates to examine their influence on the intervention effect. Secondary Outcomes: All self-reported falls, all self-reported fall-related injuries, and measures of well-being.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Accidental Falls, Wounds and Injuries

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
5451 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Fall prevention standard of care
Arm Type
Other
Arm Description
An evidence-based patient-centered intervention that will combine elements of a multifactorial, risk factor-based, standardly-tailored fall prevention strategy developed at Yale, practice guidelines offered by the CDC's "STEADI" toolbox and the joint American Geriatrics Society/British Geriatrics Society guidelines, and ACOVE practice change approach
Arm Title
Control
Arm Type
Other
Arm Description
Usual fall prevention care
Intervention Type
Other
Intervention Name(s)
Evidence-based tailored fall prevention
Intervention Type
Other
Intervention Name(s)
Usual care
Primary Outcome Measure Information:
Title
First Adjudicated Serious Fall-Related Injury
Description
Number of first adjudicated serious fall-related injury serious fall-related injury events per 100 per years of follow-up.
Time Frame
Enrollment through last completed follow-up or death interview (max 44 months)
Secondary Outcome Measure Information:
Title
First Self-reported Fall-related Injury
Description
Number of first self-reported fall-related injuries per 100 per years of follow-up
Time Frame
Enrollment through last completed follow-up or death interview (max 44 months)
Title
Time to Self-reported Falls
Description
** data for this outcome was not collected
Time Frame
these data were not collected
Title
Physical Function
Description
Late Life Function and Disability Instrument (LL-FDI) function score. The scores are on a 0-100 scale, higher score = better function. The measure reported is the mean of scores at the 12-month and 24-months follow-up assessment
Time Frame
measured at 12-month and 24-month follow-up assessments, reported score is an average (mean) of the follow-up scores
Title
Disability
Description
Late Life Function and Disability Instrument (LL-FDI) disability score. The scores are on a 0-100 scale, higher score = less disability. The measure reported is the mean of scores at the 12-month and 24-months follow-up assessment
Time Frame
measured at 12-month and 24-month follow-up assessments, reported score is an average (mean) of the follow-up scores
Title
Anxiety
Description
Patient-reported Outcome Measure Information System (PROMIS) Anxiety subscale. Measured on a 8-40 Scale, higher score = more anxiety.
Time Frame
Measured at 12-month and 24-month follow-up assessments, reported score is an average (mean) of the follow-up scores.
Title
Depression
Description
PROMIS depression subscale. Measured on a 8-40 Scale, higher score = more depression.
Time Frame
Measured at 12-month and 24-month follow-up assessments, reported score is an average (mean) of the follow-up scores.
Title
Fear of Falling
Description
Falls Efficacy Scale. Measured on a 10-40 Scale, higher score = more fear of falling.
Time Frame
Measured at 12-month and 24-month follow-up assessments, reported score is an average (mean) of the follow-up scores.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: The patient is at least 70 years of age. The patient must answer 'yes' to one or more of the following questions: Have you fallen and hurt yourself in the past year? Have you fallen 2 or more times in the past year? Are you afraid that you might fall because of balance or walking problems? Exclusion Criteria: The patient is enrolled in hospice. The patient resides in a nursing home. The patient is not capable of providing informed consent (or assent), and a proxy is not available. The patient does not speak English or Spanish
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shalender Bhasin, MD
Organizational Affiliation
Brigham and Women's Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Thomas Gill, MD
Organizational Affiliation
Yale University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Dave Reuben, MD
Organizational Affiliation
University of California, Los Angeles
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Nancy Latham, PhD
Organizational Affiliation
Brigham and Women's Hosptial
Official's Role
Study Director
Facility Information:
Facility Name
Healthcare Partners
City
Torrance
State/Province
California
Country
United States
Facility Name
University of Iowa Health Alliance
City
Des Moines
State/Province
Iowa
Country
United States
Facility Name
Johns Hopkins Medicine
City
Baltimore
State/Province
Maryland
Country
United States
Facility Name
Partners Healthcare
City
Boston
State/Province
Massachusetts
Country
United States
Facility Name
Reliant Medical Group
City
Worcester
State/Province
Massachusetts
Country
United States
Facility Name
University of Michigan
City
Ann Arbor
State/Province
Michigan
Country
United States
Facility Name
Essentia Health
City
Duluth
State/Province
Minnesota
Country
United States
Facility Name
Mt Sinai Health System
City
New York
State/Province
New York
Country
United States
Facility Name
University of Pittsburgh
City
Pittsburgh
State/Province
Pennsylvania
Country
United States
Facility Name
University of Texas Medical Branch at Galveston
City
Galveston
State/Province
Texas
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
35932279
Citation
Ganz DA, Yuan AH, Greene EJ, Latham NK, Araujo K, Siu AL, Magaziner J, Gurwitz JH, Wu AW, Alexander NB, Wallace RB, Greenspan SL, Rich J, Volpi E, Waring SC, Dykes PC, Ko F, Resnick NM, McMahon SK, Basaria S, Wang R, Lu C, Esserman D, Dziura J, Miller ME, Travison TG, Peduzzi P, Bhasin S, Reuben DB, Gill TM. Effect of the STRIDE fall injury prevention intervention on falls, fall injuries, and health-related quality of life. J Am Geriatr Soc. 2022 Nov;70(11):3221-3229. doi: 10.1111/jgs.17964. Epub 2022 Aug 6.
Results Reference
derived
PubMed Identifier
33678038
Citation
Esserman DA, Gill TM, Miller ME, Greene EJ, Dziura JD, Travison TG, Meng C, Peduzzi PN. A case study of ascertainment bias for the primary outcome in the Strategies to Reduce Injuries and Develop Confidence in Elders (STRIDE) trial. Clin Trials. 2021 Apr;18(2):207-214. doi: 10.1177/1740774520980070. Epub 2021 Mar 7.
Results Reference
derived
PubMed Identifier
33037632
Citation
Gill TM, Bhasin S, Reuben DB, Latham NK, Araujo K, Ganz DA, Boult C, Wu AW, Magaziner J, Alexander N, Wallace RB, Miller ME, Travison TG, Greenspan SL, Gurwitz JH, Rich J, Volpi E, Waring SC, Manini TM, Min LC, Teresi J, Dykes PC, McMahon S, McGloin JM, Skokos EA, Charpentier P, Basaria S, Duncan PW, Storer TW, Gazarian P, Allore HG, Dziura J, Esserman D, Carnie MB, Hanson C, Ko F, Resnick NM, Wiggins J, Lu C, Meng C, Goehring L, Fagan M, Correa-de-Araujo R, Casteel C, Peduzzi P, Greene EJ. Effect of a Multifactorial Fall Injury Prevention Intervention on Patient Well-Being: The STRIDE Study. J Am Geriatr Soc. 2021 Jan;69(1):173-179. doi: 10.1111/jgs.16854. Epub 2020 Oct 9.
Results Reference
derived
PubMed Identifier
32640131
Citation
Bhasin S, Gill TM, Reuben DB, Latham NK, Ganz DA, Greene EJ, Dziura J, Basaria S, Gurwitz JH, Dykes PC, McMahon S, Storer TW, Gazarian P, Miller ME, Travison TG, Esserman D, Carnie MB, Goehring L, Fagan M, Greenspan SL, Alexander N, Wiggins J, Ko F, Siu AL, Volpi E, Wu AW, Rich J, Waring SC, Wallace RB, Casteel C, Resnick NM, Magaziner J, Charpentier P, Lu C, Araujo K, Rajeevan H, Meng C, Allore H, Brawley BF, Eder R, McGloin JM, Skokos EA, Duncan PW, Baker D, Boult C, Correa-de-Araujo R, Peduzzi P; STRIDE Trial Investigators. A Randomized Trial of a Multifactorial Strategy to Prevent Serious Fall Injuries. N Engl J Med. 2020 Jul 9;383(2):129-140. doi: 10.1056/NEJMoa2002183.
Results Reference
derived
PubMed Identifier
32408769
Citation
Esserman D. From screening to ascertainment of the primary outcome using electronic health records: Challenges in the STRIDE trial. Clin Trials. 2020 Aug;17(4):346-350. doi: 10.1177/1740774520920898. Epub 2020 May 14.
Results Reference
derived
PubMed Identifier
32212395
Citation
Gill TM, McGloin JM, Shelton A, Bianco LM, Skokos EA, Latham NK, Ganz DA, Nyquist LV, Wallace RB, Carnie MB, Dykes PC, Goehring LA, Doyle M, Charpentier PA, Greene EJ, Araujo KL. Optimizing Retention in a Pragmatic Trial of Community-Living Older Persons: The STRIDE Study. J Am Geriatr Soc. 2020 Jun;68(6):1242-1249. doi: 10.1111/jgs.16356. Epub 2020 Mar 25.
Results Reference
derived
PubMed Identifier
31245263
Citation
Ganz DA, Siu AL, Magaziner J, Latham NK, Travison TG, Lorenze NP, Lu C, Wang R, Greene EJ, Stowe CL, Harvin LN, Araujo KLB, Gurwitz JH, Agrawal Y, Correa-De-Araujo R, Peduzzi P, Gill TM; STRIDE Investigators. Protocol for serious fall injury adjudication in the Strategies to Reduce Injuries and Develop Confidence in Elders (STRIDE) study. Inj Epidemiol. 2019 Apr 15;6:14. doi: 10.1186/s40621-019-0190-2. eCollection 2019.
Results Reference
derived
PubMed Identifier
30020415
Citation
Gill TM, McGloin JM, Latham NK, Charpentier PA, Araujo KL, Skokos EA, Lu C, Shelton A, Bhasin S, Bianco LM, Carnie MB, Covinsky KE, Dykes P, Esserman DA, Ganz DA, Gurwitz JH, Hanson C, Nyquist LV, Reuben DB, Wallace RB, Greene EJ. Screening, Recruitment, and Baseline Characteristics for the Strategies to Reduce Injuries and Develop Confidence in Elders (STRIDE) Study. J Gerontol A Biol Sci Med Sci. 2018 Oct 8;73(11):1495-1501. doi: 10.1093/gerona/gly076.
Results Reference
derived

Learn more about this trial

Strategies to Reduce Injuries and Develop Confidence in Elders

We'll reach out to this number within 24 hrs