- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04845789
Case Manager Approach in Dementia Care From a Caregiver Perspective
Case Manager Approach in Dementia Care From a Caregiver Perspective: A Grounded Theory Study
Study Overview
Detailed Description
This was a qualitative study using semi-structured interviews with caregivers of community-dwelling people with dementia. Purposive sampling was used to recruit caregivers from Jockey Club Centre for Positive Ageing.
Study protocol would be explained by principal investigator (PI) to case managers in JCCPA, including aim and objectives of the study, inclusion criteria, exclusion criteria and interview questions.
Due to privacy issues, case managers in JCCPA would screen family caregivers and ask for consent to participate in the study. Contact method of caregivers would be provided to PI by JCCPA case managers upon caregivers' consent. PI would then approach caregivers to arrange online meetings and send the online consent form to them for their consideration and reference. Risks and benefits of the study and the right to withdraw from the study at any time would be explained to participants before consent form was signed by participants digitally.
Demographic data such as age, gender, education level, years of caregiving to PWD and time spent on caregiving would be collected using Google form.
All interviews were conducted through video-conferencing individually. Each interview took 30 to 45 minutes. The interviews were started with an close-ended question, such as "Do you know the special approach that JCCPA has adopted?" and "Did the staff tell you about it at admission?", followed up by open-ended questions such as "What do you know about case management?" and "Can you tell me how your caregiving experience was with case manager support?". Subsequent probing questions aimed at clarification and gaining more insight on their experience, was guided by the participant's responses.
Demographic data such as age, gender, education level, years of caregiving to PWD and time spent on caregiving would be collected using Google form.
All interviews were conducted through video-conferencing individually. Each interview took 30 to 45 minutes. The interviews were started with an close-ended question, such as "Do you know the special approach that JCCPA has adopted?" and "Did the staff tell you about it at admission?", followed up by open-ended questions such as "What do you know about case management?" and "Can you tell me how your caregiving experience was with case manager support?". Subsequent probing questions aimed at clarification and gaining more insight on their experience, was guided by the participant's responses. Video-conferencing software such as Zoom, Google Meet, or facetime would be used for online interview. Interview would be conducted in JCCPA to ensure privacy of the participants.
All interviews were audio recorded and transcribed verbatim. The transcript were validated by re-listening to the tapes.
Constant comparative analysis was used for coding and category development. Incidents were identified in the data and coded. Initially, codes were identified as much as possible. Codes were compared to others codes. Codes were then collapsed into categories. In this process, incidents in a category were compared with previous incidents. New data was compared with data obtained earlier during the analysis phases. In intermediate coding, basic data was transformed into more abstract concepts allowing the theory to emerge from the data. Then, advanced coding was done to facilitate integration of the final grounded theory.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Kam Yan Lui, Miss
- Phone Number: +85263329630
- Email: 1155138933@link.cuhk.edu.hk
Study Locations
-
-
NT
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Shatin, NT, Hong Kong, 0000
- Jockey Club Centre for Positive Ageing
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Contact:
- Andrew Cheung, Mr
- Phone Number: +85253456773
- Email: info@jccpa.org.hk
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- care recipients having clinical diagnosis of dementia of any stage
- participants being the family caregivers of care recipients, providing care for at least 10 hours per week
- caregivers receiving case manager support for at least 3 months
Exclusion Criteria:
- caregivers who were under age of 18 and those exhibiting intellectual impairment
- caregivers who were not immediate family members of care recipients
- caregivers who could not communicate in Cantonese or English
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Family caregivers
Family caregivers who were main caregiver to the person with dementia and who spent at least 10 hours a week providing care to the person with dementia.
|
Non-interventional.
Interview would be conducted for data collection.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Semi-structured interview would be conducted individually
Time Frame: 2/5/2021-31/7/2021
|
for data collection to explore the perspective of family caregivers on case manager approach in dementia care.
|
2/5/2021-31/7/2021
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Kam Yan Lui, Miss, Chinese University of Hong Kong
Study record dates
Study Major Dates
Study Start (Anticipated)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- CaseManagerDementiaGT
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- CSR
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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