Evaluation and Development of Falls Prevention and Management in the Community for Older Adults

April 6, 2022 updated by: Noah Lim, National University, Singapore

Evaluation and Development of Falls Prevention and Management in the Community of Central and North of Singapore for Older Adults

This study investigates how differently-framed messages can affect people's attitude towards falls risk and prevention in older adults. This study considers the potentiality of adult children acting as change agents in influencing parents in falls prevention.

Study Overview

Detailed Description

A randomized controlled trial (RCT) will be conducted to test the effectiveness of two messaging types (positively vs negatively framed) via two target audiences (older vs younger adults).

The RCT evaluates the effectiveness of the differently-framed messages delivered to older and younger adults in affecting people's attitude toward falls risk and motivating them to learn about preventing falls. Also, the potential of adult children acting as change agents to positively influence parents in preventing falls is explored.

Older and younger adults who are eligible to participate in this study are randomly given one message. For older adults, the objective is to study which message is more effective in affecting their attitude towards falls risk and motivating them to learn about preventing falls. For younger adults, the aim is to understand which message is more effective in motivating them to learn about preventing falls for their parents.

Hypotheses:

H1: The negatively framed message is more effective than the positively framed counterpart in motivating older adults to find out about preventing falls. However, this effect decreases as the socioeconomic status decreases.

H2: The negatively framed message is more effective than the positively framed counterpart in motivating younger adults to find out about preventing falls.

Study Type

Interventional

Enrollment (Anticipated)

1200

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 Contact

Study Contact Backup

Study Locations

      • Singapore, Singapore
        • Recruiting
        • National University of Singapore
        • Contact:

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

30 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Singaporean or Permanent Residents (PRs)
  • Read/speak English, Mandarin, or Malay
  • Either age 60 years old and above, walk independently with or without assistive devices, have no self-reported/detected dementia or cognitive impairments or age between 30 and 59 years old and have either one of the parents age 60 years old and above who walk independently with or without assistive devices

Exclusion Criteria:

  • Not Singaporean or PRs
  • Do not read/speak English, Chinese, and Malay
  • Age 29 years old and below
  • Cannot walk independently with and without assistive devices
  • Have self-reported/detected dementia or cognitive impairments

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: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Control - Older Adults
Participants age 60 years old or above.
Participants in this arm are not given any intervention.
Experimental: Positive - Older Adults
Participants age 60 years old or above.
Participants in this arm are given a positively framed message from an older adult's point of view.
Experimental: Negative - Older Adults
Participants age 60 years old or above.
Participants in this arm are given a negatively framed message from an older adult's point of view.
Experimental: Control - Younger Adults
Participants age between 30 and 59 years old.
Participants in this arm are not given any intervention.
Experimental: Positive - Younger Adults
Participants age between 30 and 59 years old.
Participants in this arm are given a positively framed message from an adult child's point of view.
Experimental: Negative - Younger Adults
Participants age between 30 and 59 years old.
Participants in this arm are given a negatively framed message from an adult child's point of view.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
How much does the participant want to find out about preventing falls for himself/herself or his/her father/mother?
Time Frame: After being given a message during the survey, an average of 2 minutes
This is a scale variable ranging from 1 to 9, which is "1" if not at all and "9" if a lot
After being given a message during the survey, an average of 2 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Whether the participant or the participant's father/mother has fallen in the past 12 months
Time Frame: After being given a message during the survey, an average of 2 minutes
This is a categorical variable, which is "Yes" if the participant or the participant's father/mother has fallen in the past 12 months, "No" if not, and "Do not know" if the participant does not know whether his/her father/mother has fallen in the past 12 months
After being given a message during the survey, an average of 2 minutes
Whether the participant or the participant's father/mother is concerned about falling
Time Frame: After being given a message during the survey, an average of 2 minutes
This is a categorical variable, which is "Very concerned" if the participant or the participant's father/mother is very concerned about falling, "Slightly concerned" if s/he is slightly concerned about falling, "Not concerned" if s/he is not concerned about falling, and "Do not know" if the participant does not know whether his/her father/mother is concerned about falling
After being given a message during the survey, an average of 2 minutes
Whether the participant or the participant's father/mother feels like s/he is going to fall when standing or walking
Time Frame: After being given a message during the survey, an average of 2 minutes
This is a categorical variable, which is "Always" if the participant or the participant's father/mother always feels like s/he is going to fall when standing or walking, "Sometimes" if s/he sometimes feels like s/he is going to fall when standing or walking, "Never" if s/he never feels like s/he is going to fall when standing or walking, and "Do not know" if the participant does not know whether his/her father/mother feels like s/he is going to fall when standing or walking
After being given a message during the survey, an average of 2 minutes

Collaborators and Investigators

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

Investigators

  • Study Director: Noah Lim, PhD, The Global Asia Institute, The National University of Singapore
  • Principal Investigator: Tuo-Yu Chen, PhD, Master Program in Global Health and Development, Taipei Medical University
  • Principal Investigator: Su-Chin Hsu, PhD, The Global Asia Institute, The National University of Singapore
  • Principal Investigator: Lianjun Li, PhD, The Global Asia Institute, The National University of Singapore
  • Principal Investigator: Catherine Yeung, PhD, Department of Marketing, The Chinese University of Hong Kong

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 (Actual)

December 10, 2021

Primary Completion (Anticipated)

September 30, 2022

Study Completion (Anticipated)

September 30, 2022

Study Registration Dates

First Submitted

December 7, 2021

First Submitted That Met QC Criteria

January 15, 2022

First Posted (Actual)

January 20, 2022

Study Record Updates

Last Update Posted (Actual)

April 14, 2022

Last Update Submitted That Met QC Criteria

April 6, 2022

Last Verified

April 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • NUS-IRB-2020-024

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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