Community-based Falls Prevention Program for the Elderly

September 4, 2015 updated by: Dr. David Matchar, National University, Singapore

Multifactorial, Evidence-based Program of Screening, Risk Modification and Physical Therapy to Prevent Falls Among Vulnerable Elderly Recently Discharged From Hospital to the Community.

Background: Falls are the leading cause of injury among older adults in Singapore, but falls among the elderly can be preventable and the risks are predictable. Translating this understanding of falls etiology into an integrated clinical and public health program that is accessible to the elderly is a critical health services delivery challenge.

Hypothesis: An evidence-based program of screening, risk modification and physical therapy delivered in a community setting will reduce recurrent falls incidence among a high-risk group of elderly recently discharged to the community.

Methodology: This randomized controlled trial targets patients seen at Emergency Department (ED) for a fall or fall-related injuries who are at least 65 years old and will be discharged to home. Upon signing the informed consent form, the participants will be followed up for nine months from the baseline assessment during which the participants are randomized into either a control or the intervention group. The participants in the intervention group will be provided with a multifactorial program of screening, risk modification and physical therapy focused on progressive strength, balance, and gait training either as an individualized program or a group setting in the community for the first three months from the date of randomization. The number of recurrent falls will be monitored via a falls prevention diary maintained by (or for) each participant.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Objective:

To develop and demonstrate the feasibility and effectiveness of a multifactorial, community-based falls prevention program of screening, risk modification, and progressive physical therapy that targets vulnerable elderly Singaporeans at high-risk of falls.

Methodology:

This two-year, multi-center, two-arm, parallel group, randomized controlled trial will be divided into three phases: (1) pre-study, (2) intervention, and (3) analysis.

During the pre-study phase, overseas experts will train local physiotherapists and community health workers on how to administer and deliver the falls prevention program. Engaging hospital-based physiotherapists to deliver the home-based assessments and exercise programs will maximize the likelihood of long-term sustainability of the intervention program. In addition, manuals will be developed for physiotherapists to guide the evaluation risk factor assessments, home environment assessments, appropriate referrals to different health care providers, and selection of exercise programs that will be progressive, challenging and of optimal intensity and durations. Manuals for risk factor assessments will be shared with the blinded assessors.

The intervention phase will be divided into two phases: a three-month "Active Intervention Phase" and a six-month "Maintenance Phase." In the beginning of the active intervention phase, the participants in the intervention group will receive a detailed falls risk assessment at the baseline assessment by a physiotherapist. The risk factors that will be assessed are the following:

  1. Poor vision: Referral to ophthalmologist for correction
  2. Polypharmacy: Referral to AIC for management of medications if use of five or more medications
  3. Environmental Hazards: Caregiver education and suitable recommendations according to the CDC guidelines to modify risk such as removal of rugs, change to safer footwear, use of non-slip bath mats, additional lighting at night.
  4. Deficiencies in gait, balance or mobility: Physiotherapist-supervised program of gait training, balance and strengthening exercises In the analysis phase, the collected data will be analyzed. The primary outcome measure of the study is the number of fallers over the entire study period. The number of falls will be captured by a falls prevention diary maintained by (or for) each participant.

Procedures:

The elderly seen at ED for a fall or fall-related injury will be screened for participation of the study. Once the consent is taken, all study participants will be given an assessment by a physiotherapist at baseline which assesses sociodemographic characteristics, functional status measured by the Short Physical Performance Battery (SPPB), two-minute walk test, history of falls, cognitive impairment measured by the Montreal Cognitive Assessment (MoCA), quality of life (EQ-5D-5L and EQ-VAS), health care utilization, and medical history (polypharmacy, orthostatic vital signs, and self-reporting eyesight and hearing).

At the end of baseline assessment, the participants will be assigned either a control or the intervention group. Before the start of the exercise sessions, the participants in the intervention group will. Need to complete Physical Activity Readiness Questionnaire (PAR-Q) and a medical evaluation by a physician to ensure that the participants are fit for physical activity. Based on the SPPB score at baseline assessment, participants will be categorized as either high-risk (SPPB<6) or low-to-moderate-risk (SPPB>6) for falls. High-risk patients will be given an individualized PT-supervised program of physical therapy that specifically targets impairments that interfere with engaging in exercise in group setting. The goal of the tailored physical therapy sessions is to modify impairments and transition these patients to an evidence-based exercise program. Low-to-moderate-risk patients will be directly enrolled into an evidence-based group exercise program. The group exercise programs will be offered as one-hour sessions, twice weekly over the intervention period. At the end of the active intervention phase, these participants will transition to a maintenance phase in which they will be encouraged to continue with the exercise on their own and will also be referred to the Health Promotion Board's STEP program.

The participants will be asked at the end of the active intervention phase (three months from the date of randomization) and at the end of the study period (nine months from the date of randomization) about their functional status, history of falls, cognitive impairment, quality of life, health care utilization, and medical history by the blinded assessors. Recurrent falls incidence will be monitored by participants' self-reporting monthly falls diary as well as monthly phone calls conducted by the study coordinator during the entire study period.

Study Type

Interventional

Enrollment (Actual)

354

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Singapore, Singapore, 169608
        • Singapore General Hospital
      • Singapore, Singapore, 529889
        • Changi General Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

65 years and older (OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Age ≥ 65 years
  • Seen in the Emergency Department for a fall or injury related to a fall
  • Able to follow 3 step commands
  • Singapore citizen or Permanent Resident
  • Living at home upon discharge
  • Provision of informed consent
  • If admitted to the hospital, the illness or disability is one from which they are expected to recover basic ADLs or weight bearing of the lower extremity within the next month

Exclusion Criteria:

  • Those patients with severe physical and/or mental impairments which preclude participation in a program of physical therapy (as determined by a primary physician) will NOT be eligible for participation.
  • Unable to participate in the exercise program due to conflicting schedules (e.g. full-time employment, on dialysis)
  • Serious life limiting illness
  • Patients seen at ED due to road traffic accidents
  • Unable to walk even with assistance
  • Not community dwelling prior to ED visit
  • Total blindness
  • Needs emergency inpatient surgery and, if admitted to the hospital, the illness or disability is one from which they are not expected to recover basic ADLs or weight bearing in the lower extremity within the next one month.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: PREVENTION
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Intervention Group
The intervention consists of a tailored physical therapy focused on progressive strength, balance and gait training for a period of 3 months.
Tailored physical therapy sessions to modify impairments in balance and/or gait and to transition high-risk participants to an evidence-based group exercise program.
Other Names:
  • Falls Prevention
NO_INTERVENTION: Control Group
Usual care by physician.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
The number of fallers who have fallen at least once during the 9-month study period
Time Frame: 9 months
9 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The number of injurious falls and healthcare utilization
Time Frame: 9 months
Injurious falls are the falls that resulted in participants' seeking medical attention or restricting their daily activities for at least 48 hours.
9 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

December 1, 2012

Primary Completion (ACTUAL)

April 1, 2015

Study Registration Dates

First Submitted

October 22, 2012

First Submitted That Met QC Criteria

October 22, 2012

First Posted (ESTIMATE)

October 24, 2012

Study Record Updates

Last Update Posted (ESTIMATE)

September 7, 2015

Last Update Submitted That Met QC Criteria

September 4, 2015

Last Verified

September 1, 2015

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • HSRG10MAY002

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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