- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03233971
How do Older Adults and Caregivers Feel About Their Medications?
April 3, 2018 updated by: Kua Chong Han, Monash University
Patients' and Caregivers' Attitudes Towards Deprescribing in the Asian Community Setting
The aim of this study is to study patients' and caregivers' perspectives towards deprescribing using the Revised Patients' Attitudes Towards Deprescribing (rPATD) questionnaire.
Study Overview
Study Type
Observational
Enrollment (Actual)
1057
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
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Singapore, Singapore
- Multi-centres
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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
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Potential participants will be selected by convenient sampling from walk-in patients/caregivers who present at the participating pharmacies seeking advice or medication.
Description
Inclusion Criteria:
Older adults' inclusion criteria:
- age at least 65 years;
- taking one or more long-term prescription medication;
- have not participated in this anonymous questionnaire previously
Caregivers' inclusion criteria:
- currently an informal caregiver for an older adult (defined as having any role in a family member or friend's management of health and/or medications);
- care recipient must be at least 65 years of age and taking one or more long-term prescription medication;
- have not participated in this anonymous questionnaire previously
Exclusion Criteria:
Older adults' exclusion criteria:
- inability to complete a questionnaire in English.
Caregivers' exclusion criteria:
- caregiver's age less than 21 years;
- caregiver's inability to complete a questionnaire in English.
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
- Observational Models: Other
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Older adults
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A 5-point Likert scale questionnaire consisting of 22 questions for older adults, and 19 questions of caregivers.
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Caregivers
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A 5-point Likert scale questionnaire consisting of 22 questions for older adults, and 19 questions of caregivers.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
rPATD questionnaire scorings
Time Frame: up to 9 months
|
up to 9 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this 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)
July 25, 2017
Primary Completion (Actual)
March 30, 2018
Study Completion (Actual)
March 30, 2018
Study Registration Dates
First Submitted
July 24, 2017
First Submitted That Met QC Criteria
July 27, 2017
First Posted (Actual)
July 31, 2017
Study Record Updates
Last Update Posted (Actual)
April 4, 2018
Last Update Submitted That Met QC Criteria
April 3, 2018
Last Verified
April 1, 2018
More Information
Terms related to this study
Other Study ID Numbers
- 2017-8872
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
product manufactured in and exported from the U.S.
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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