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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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05081570
Enrollment
78
Registered
2021-10-18
Start date
2021-10-30
Completion date
2023-07-30
Last updated
2023-09-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Keywords

stroke, telecare consultation, nurse clinic

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.

Detailed description

The aim of this pilot study is to determine the feasibility and effectiveness of telecare consultation in nurse-led post-acute stroke clinic. Method: The present pilot study adopts a one-group pre-test post-test design. The potential subjects will be recruited from the clinic in Queen Elizabeth Hospital if they are (1) having a confirmed diagnosis of stroke within 1 month before enrolment, (2) referred to nurse-led post-acute stroke clinic, (3) aged 18 or above, (4) cognitively competent with a score ≥ 22 in the Montreal Cognitive Assessment Hong Kong version, (5) living at home before and after discharged from the acute stroke unit, and (6) having a smartphone or living with family member who has a smartphone. The participants will receive two tertiary stroke care consultations provided by stroke nurses via telecare in 2 months. The outcome measures include feasibility (reasons for refusal and drop-out, acceptance and satisfaction of both the advanced practising nurses and their patients towards the program), and effectiveness (degree of disability after stroke, activity of daily living, instrumental activity of daily living, health-related quality of life, depression). Data will be collected at pre- (T1) and post- (T2) intervention. Discussion: The findings of this pilot study can provide a preliminary evidence on the use of telecare consultation in the nurse-led post-acute stroke clinic including its feasibility and effectiveness on both providers and patients. When gaps are identified, they could be adjusted to help develop and design a definitive, large-scale randomized controlled trial.

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.

Sponsors

The Queen Elizabeth Hospital
CollaboratorOTHER
The Hong Kong Polytechnic University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Masking description

No masking is needed

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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 * no Internet connection at home * participating in other clinical trials at the same time * require physical contact, i.e. wound dressing

Design outcomes

Primary

MeasureTime frameDescription
Degree of disability after strokebaseline, three months when the program is completedSimplified modified Rankin scale will be used to measure the degree of disability for stroke patients.

Secondary

MeasureTime frameDescription
Post-stroke depressionbaseline, three months when the program is completedPost-stroke depression will be measured using the Chinese version of the Geriatric Depression Scale
Medication adherencebaseline, three months when the program is completedMedication adherence will be determined using the Adherence to Refills and Medications Scale (ARMS).
Social participationbaseline, three months when the program is completedSocial 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.
Number of attendances at a general practitioner's office, emergency department, hospital, and general out-patient clinicbaseline, three months when the program is completedTo measure the utilization of healthcare services by stroke patient before and after the intervention.
Quality of lifebaseline, three months when the program is completedQuality of life will be measured using the Hong Kong version of EuroQol 5-dimension (EQ-5D-5L).

Other

MeasureTime frameDescription
the success of the adoption of telecare consultationthree months when the program is completedthe Readiness for Implementation Model Survey will be used to evaluate the success of the adoption of telecare consultation at the staff and clinic level. This 42-item survey centers on attitudes, organizational environment, technology usefulness factors, and implementation process factors.
IT literacybaseline, three months when the program is completedIT literacy will be assessed by answering the question, How confident are you in using a smartphone to have meetings with others? using a 5-point scale where 1=not very confident, and 5=very confident.
Number of patients who are eligible, excluded, recruited, and completed.three months when the program is completedTo assess the feasibility of the program to the stroke patients

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026