- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05198193
Evaluation and Development of Falls Prevention and Management in the Community for Older Adults
Evaluation and Development of Falls Prevention and Management in the Community of Central and North of Singapore for Older Adults
Study Overview
Status
Conditions
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
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Su-Chin Hsu, PhD
- Phone Number: +6566011672
- Email: schsu@nus.edu.sg
Study Contact Backup
- Name: Lianjun Li, PhD
- Phone Number: +6566011672
- Email: lianjun.li@nus.edu.sg
Study Locations
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-
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Singapore, Singapore
- Recruiting
- National University of Singapore
-
Contact:
- Su-Chin Hsu
- Phone Number: +6566011672
- Email: schsu@nus.edu.sg
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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.
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Experimental: Positive - Older Adults
Participants age 60 years old or above.
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Participants in this arm are given a positively framed message from an older adult's point of view.
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Experimental: Negative - Older Adults
Participants age 60 years old or above.
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Participants in this arm are given a negatively framed message from an older adult's point of view.
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Experimental: Control - Younger Adults
Participants age between 30 and 59 years old.
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Participants in this arm are not given any intervention.
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Experimental: Positive - Younger Adults
Participants age between 30 and 59 years old.
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Participants in this arm are given a positively framed message from an adult child's point of view.
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Experimental: Negative - Younger Adults
Participants age between 30 and 59 years old.
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Participants in this arm are given a negatively framed message from an adult child's point of view.
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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
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After being given a message during the survey, an average of 2 minutes
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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
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After being given a message during the survey, an average of 2 minutes
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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
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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
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After being given a message during the survey, an average of 2 minutes
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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
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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
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After being given a message during the survey, an average of 2 minutes
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Collaborators and Investigators
Sponsor
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
General Publications
- Dickinson A, Machen I, Horton K, Jain D, Maddex T, Cove J. Fall prevention in the community: what older people say they need. Br J Community Nurs. 2011 Apr;16(4):174-80.
- Liu X, Shuster MM, Mikels JA, Stine-Morrow EAL. Doing What Makes You Happy: Health Message Framing for Younger and Older Adults. Exp Aging Res. 2019 Jul-Sep;45(4):293-305. doi: 10.1080/0361073X.2019.1627491. Epub 2019 Jun 12.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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