Telecare Consultation in Nurse-led Post-acute Stroke Clinic
A Pilot Study to Evaluate the Feasibility and Effectiveness of Telecare Consultation in Nurse-led Post-acute Stroke Clinic
1 other identifier
interventional
78
1 country
1
Brief Summary
Introduction: The progress of stroke recovery is slow and enduring. If stroke survivors are not properly managed to facilitate their rehabilitation after discharged from hospital, their risk for recurrence after an index stroke will be very high. Globally, nurse-led post-acute stroke clinics have been developed to provide tertiary care services to support stroke survivors. While synthesized evidence supports the idea that the post-stroke services delivered by nurses in the clinic can improve the functional ability and reduce the readmission rate, shortcomings of these services such as compulsory traveling time and cost, long waiting time at the clinic, and the pandemic situation limit the clinic utilization by stroke survivors. Telecare consultation is a new modality aiming to provide a new healthcare access experience to the public, though how it can be applied in nurse-led clinic and what effects it can bring about on post-stroke survivors has not been reported.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable stroke
Started Oct 2021
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 6, 2021
CompletedFirst Posted
Study publicly available on registry
October 18, 2021
CompletedStudy Start
First participant enrolled
October 30, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 30, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
July 30, 2023
CompletedSeptember 22, 2023
September 1, 2023
1.7 years
October 6, 2021
September 20, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Degree of disability after stroke
Simplified modified Rankin scale will be used to measure the degree of disability for stroke patients.
baseline, three months when the program is completed
Secondary Outcomes (5)
Quality of life
baseline, three months when the program is completed
Post-stroke depression
baseline, three months when the program is completed
Medication adherence
baseline, three months when the program is completed
Social participation
baseline, three months when the program is completed
Number of attendances at a general practitioner's office, emergency department, hospital, and general out-patient clinic
baseline, three months when the program is completed
Other Outcomes (3)
Number of patients who are eligible, excluded, recruited, and completed.
three months when the program is completed
IT literacy
baseline, three months when the program is completed
the success of the adoption of telecare consultation
three months when the program is completed
Study Arms (1)
Intervention group
EXPERIMENTALThe participants will receive two tertiary stroke care consultations provided by stroke nurses via telecare in 2 months.
Interventions
Two tertiary stroke care consultations will be provided by stroke nurses via telecare in 2 months. Consultation content includes provide education on modifying stroke-specific risk factors, disseminate self-management knowledge, reinforce the importance of medication compliance, revise the blood and investigation results, and co-design and follow-up on mutually agreed rehabilitation goals with the subjects. When necessary, the nurse will also refer the stroke survivors to multidisciplinary team members according to the referral guidelines. The nurse will also encourage the patients' family and/or informal caregivers to participate in the consultations.
Eligibility Criteria
You may qualify if:
- confirmed diagnosis of stroke within 1 month before enrolment
- will be discharged home within a week
- aged 18 or above
- cognitively competent with a score equal to or greater than 22 in the Montreal Cognitive Assessment Hong Kong version
- own a smartphone
You may not qualify if:
- have unaccompanied hearing or vision loss
- cannot be reached by phone
- bedbound
- no Internet connection at home
- participating in other clinical trials at the same time
- require physical contact, i.e. wound dressing
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- The Hong Kong Polytechnic Universitylead
- The Queen Elizabeth Hospitalcollaborator
Study Sites (1)
Queen Elizabeth Hospital
Kowloon, Hong Kong
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Arkers Wong, Ph.D.
The Hong Kong Polytechnic University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Masking Details
- No masking is needed
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant professor
Study Record Dates
First Submitted
October 6, 2021
First Posted
October 18, 2021
Study Start
October 30, 2021
Primary Completion
July 30, 2023
Study Completion
July 30, 2023
Last Updated
September 22, 2023
Record last verified: 2023-09
Data Sharing
- IPD Sharing
- Will not share