Improving Post-acute Stroke Follow-up Care by Adopting Telecare Consultations in a Nurse-led Clinic

Not Applicable

Recruiting

• Conditions: Stroke
• Interventions: Procedure: Usual face-to-face consultation; Procedure: Telecare consultation

• Registration Number: NCT05183672
• Lead Sponsor: The Hong Kong Polytechnic University

Brief Summary

Since 2017, Hong Kong has provided post-acute stroke services in clinics operated by stroke advanced practice nurses (APNs). Currently, the applicability of the clinics has been further limited by the emergence of the coronavirus (COVID-19) pandemic due to restrictions on visits to the clinics and tightened social distancing requirements. Telecare consultations may be a viable option for contributing more flexible, interactive, and cost-efficient care models to support stroke survivors over the longer run. The present study takes advantage of this opportunity by utilizing implementation science to simultaneously implement and evaluate a telecare model of care in a nurse-led post-acute stroke clinic.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2021-12-07
• Study First Submitted QC: 2022-01-05
• Study First Posted: 2022-01-10
• Study Start: 2022-12-01
• Status Verified: 2023-03
• Last Update Submitted: 2023-03-02
• Last Update Posted: 2023-03-06
• Primary Completion: 2024-06-30
• Study Completion: 2025-06-30

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 196

Inclusion Criteria

• 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

Exclusion Criteria

• have unaccompanied hearing or vision loss, cannot be reached by phone, bedbound, have no Internet connection at home, participating in other clinical trials at the same time, require physical contact, i.e. wound dressing

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Control group	Usual face-to-face consultation	Participants will receive three usual face-to-face consultations provided by stroke nurses in 3 months
Intervention group	Telecare consultation	Participants will receive three tertiary stroke care consultations provided by stroke nurses via telecare in 3 months.

Primary Outcome Measures

Name	Time	Method
Chang in Degree of disability after stroke	baseline, three months when the program is completed, three months after the program is completed.	Simplified modified Rankin scale will be used to measure the degree of disability for stroke patients. The scale has three questions to identify whether the patient has a score from 0 to 5, with higher scores representing higher degree of disability.

Secondary Outcome Measures

Name	Time	Method
Incidence of the recurrence of stroke	baseline, three months when the program is completed, three months after the program is completed.	The percentage of participants who re-admitted to hospital because of recurrent stroke
Change of Quality of life, which measures an individual perception oftheir position in life. It includes physical and mental health.	baseline, three months when the program is completed, three months after the program is completed.	Quality of life will be measured using the Hong Kong version of EuroQol 5-dimension. The scale has five subdomains, which include mobility, self-care, usual activities, pain and discomfort, and anxiety and depression. Since the scale has 5 items, each digit in the five digit codes refers to the status of each dimension, ranging from 1 for no problem, to 5 for sever problem. A higher scores indicate better quality of life.
Change of Post-stroke depression	baseline, three months when the program is completed, three months after the program is completed.	Post-stroke depression will be measured using the Chinese version of the Geriatric Depression scale. This scale has a minimum score of 0 and a maximum score of 15. Lower scores represent lower depression level.
Change of Medication adherence	baseline, three months when the program is completed, three months after the program is completed.	Medication adherence will be determined using the Adherence to Refills and Medications Scale. The scale produces an overall adherence score of 10-40, with lower scores indicating better adherence.
Change of Social participation	baseline, three months when the program is completed, three months after the program is completed.	Social participation will be measured using the 11-item Reintegration to Normal Living index. This scale is used to measure whether the patient has participated in several social activities before and after occurrence of stroke. The scale yields total score from 0-22, with higher scores indicating poorer social participation.
Number of attendances at a general practitioners' office, emergency department, hospital, and general out-patient clinic	baseline, three months when the program is completed, three months after the program is completed.	To measure the utilization of healthcare services by stroke patient before and after the intervention

Trial Locations

Locations (1)

Queen Elizabeth Hospital; 🇭🇰 Kowloon, Hong Kong