An mHealth-based Healthcare Professional-Lay Health Worker Partnership Program (mHLPP)
2 lipca 2026 zaktualizowane przez: Arkers, Wong, The Hong Kong Polytechnic University
A Feasibility Study of an mHealth-based Healthcare Professional-Lay Health Worker Partnership Program (mHLPP) Among Community-dwelling Impoverished Older Adults
The project aimed at training female food delivery workers from Food Angel to perform basic health checks for older adults living alone in the community.
After undergoing training, the female delivery workers will be equipped with basic health knowledge and the ability to measure physical vital signs, including blood oxygen levels, blood pressure, and pulse and pain indices, for around 100 older adults when they visit them to deliver meals. The health data collected by the delivery workers will be uploaded to the mHealth monitoring platform developed by Prof. Arkers Wong's research team. Registered nurses (RNs) will be given access to the platform to evaluate the health status of the older adults. When needed, an RN will give in-depth personal care and interventions via the mHealth app to the older adults. Referrals to allied health professionals or social workers can also be made by the RNs for early interventions.
The team hope that this first-of-its-kind grassroots community health model, undertaken in combination with the Health-Social Partnership, will provide scientific research evidence for the Hong Kong government to consider introducing the mHealth app and the service model to the community as a way to strengthen primary healthcare.
The mHealth app is a pilot health management mobile app with an interactive nurse support function. The app enables nurses to monitor the health status of users and allow users to communicate with nurses when they have health concerns. Research findings released by the team in March 2023 showed that older adults' use of the app for 3 to 6 months resulted in a significant increase in self-efficacy, a significant decrease in depression levels, a reduction in the use of medical services, and an improvement in quality of life.
Przegląd badań
Status
Aktywny, nie rekrutujący
Interwencja / Leczenie
Typ studiów
Interwencyjne
Zapisy (Rzeczywisty)
230
Faza
- Nie dotyczy
Kontakty i lokalizacje
Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.
Lokalizacje studiów
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Hong Kong
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Hong Kong, Hong Kong, Hongkong, 999077
- Food Angel
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Kryteria uczestnictwa
Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dorosły
- Starszy dorosły
Akceptuje zdrowych ochotników
Nie
Opis
Inclusion Criteria:
- age 60 or over
- member of the NGO (implying that they are not receiving any Government subsidize and their monthly income is less than HKD$ 6,050)
- living within the service area of the NGO
- able to sign an informed consent.
Exclusion Criteria:
- being diagnosed with dementia
- inability to communicate
- being bed-bound
- having an active psychiatric illness with recent hospital admission within the last six months
- being already engaged in other mHealth studies.
Plan studiów
Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Badania usług zdrowotnych
- Przydział: Nie dotyczy
- Model interwencyjny: Zadanie dla jednej grupy
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
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Eksperymentalny: mHealth-based Healthcare professional-Lay health worker Partnership Program (mHLPP)
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The participants are able to receive the services offered by this program.
During the six-month program, the lay health workers deliver the free meal provided by Food Angel at the participants' home and measure the participants' vital signs including blood pressure, pulse, oxygen saturation, and pain level (if any), and they upload the results to the mHealth app subsequently.
During the 6-month program, the participants receive eleven home visits from a nurse.
During the first month, the nurse visit the participants weekly.
The nurse visit the participants twice a week for two and three months.
The nurse only visit the participants once a month between the fourth and sixth month.
The nurse conduct a comprehensive health assessment and establish some health goals with the participants during the home visit.
She formulate an individual care plan, and record them on the app for the lay health worker to follow-up.
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Feasibility of the program implementation: implementation facilitators/barriers and acceptability
Ramy czasowe: At 6 months (T3) after baseline.
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Three separated semi-structured group interviews with healthcare professionals, lay health workers, and older adults will be conducted to explore their views on facilitating, hindering factors, and the acceptability of implementing the program in the community at six months.
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At 6 months (T3) after baseline.
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Feasibility of the program implementation: safety
Ramy czasowe: At 6 months (T3) after baseline.
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Incidence of report of adverse events that is encountered by the older adults, lay health workers, and healthcare professionals will be measured to assess the safety of the program.
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At 6 months (T3) after baseline.
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Feasibility of the program implementation: fidelity
Ramy czasowe: At 6 months (T3) after baseline.
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A performance checklist that developed by the research team according to the workflow of the program will be used to identify whether the program is implemented as intended.
The principal investigator of the research team will pay random quality assurance visits to evaluate whether the provided interventions are adhered to the planned content, duration, and frequency of the contact sessions.
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At 6 months (T3) after baseline.
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Feasibility of the study methods: program reach
Ramy czasowe: At 6 months (T3) after baseline.
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The number of older adults and lay health workers who are eligible, invited, excluded, and enrolled to participate in the program will be counted and compared to non-participants on key demographic data such as age, sociodemographic background, and living area.
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At 6 months (T3) after baseline.
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Feasibility of the study methods: feasibility of recruitment procedures and eligibility criteria
Ramy czasowe: At 6 months (T3) after baseline.
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The project manager of the study will be asked about the feasibility of the recruitment procedures, and the appropriateness of the eligibility criteria.
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At 6 months (T3) after baseline.
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Feasibility of the study methods: feasibility of data collection and analysis method
Ramy czasowe: At 6 months (T3) after baseline.
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The research assistants will provide feedback on the length, clarity and acceptability of focus group interview questions and quantitative questionnaires, and ease of collecting data.
The principal investigator of the research team will and review the results from the focus groups interviews for indications of important issues relating to data collection or analysis.
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At 6 months (T3) after baseline.
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Preliminary effectiveness on older adults: Blood pressure
Ramy czasowe: Baseline assessments (T1), 3 months (T2) and 6 months (T3) after baseline.
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Blood pressure measurement will be performed after 10 minutes of sitting rest.
A standard electronic sphygmomanometer will be used to measure supine blood pressure on the right arm of each candidate (unless contraindicated).
The results on blood pressure will be divided into systolic and diastolic blood pressure.
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Baseline assessments (T1), 3 months (T2) and 6 months (T3) after baseline.
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Preliminary effectiveness on older adults: HbA1c
Ramy czasowe: Baseline assessments (T1), 3 months (T2) and 6 months (T3) after baseline.
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HbA1c is a standard assessment of glycemia and refers to the mean blood glucose levels over the previous 2 to 3 months.
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Baseline assessments (T1), 3 months (T2) and 6 months (T3) after baseline.
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Preliminary effectiveness on older adults: fasting lipid
Ramy czasowe: Baseline assessments (T1), 3 months (T2) and 6 months (T3) after baseline.
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Fasting lipid profile includes cholesterol level, and high- and low-density lipoprotein.
Both HbA1c and the fasting lipid profile will be drawn from participants' blood from their fingers at the third and sixth month when nurses have the home visits.
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Baseline assessments (T1), 3 months (T2) and 6 months (T3) after baseline.
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Preliminary effectiveness on older adults: body mass index (BMI)
Ramy czasowe: Baseline assessments (T1), 3 months (T2) and 6 months (T3) after baseline.
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BMI results from dividing a subject's weight in kilograms by the square of their height in meters.
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Baseline assessments (T1), 3 months (T2) and 6 months (T3) after baseline.
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Preliminary effectiveness on older adults: quality of life
Ramy czasowe: Baseline assessments (T1), 3 months (T2) and 6 months (T3) after baseline.
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Quality of life will be measured by the version 2 of the 12-item Short Form Health Survey.
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Baseline assessments (T1), 3 months (T2) and 6 months (T3) after baseline.
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Preliminary effectiveness on older adults: perceived social support
Ramy czasowe: Baseline assessments (T1), 3 months (T2) and 6 months (T3) after baseline.
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Perceived social support will be evaluated using the 32-item Chinese version of the Perceived Social Support Scale for Older Adults.
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Baseline assessments (T1), 3 months (T2) and 6 months (T3) after baseline.
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Preliminary effectiveness on older adults: self-care ability
Ramy czasowe: Baseline assessments (T1), 3 months (T2) and 6 months (T3) after baseline.
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Self-care ability will be measured by the Chinese version of the Self-care Ability Scale for the Elderly (SASE).
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Baseline assessments (T1), 3 months (T2) and 6 months (T3) after baseline.
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Preliminary effectiveness on older adults: client empowerment
Ramy czasowe: Baseline assessments (T1), 3 months (T2) and 6 months (T3) after baseline.
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Client empowerment will be evaluated by the Chinese version of the Client Empowerment Scale (CCES).
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Baseline assessments (T1), 3 months (T2) and 6 months (T3) after baseline.
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Preliminary effectiveness on older adults: health service utilization
Ramy czasowe: Baseline assessments (T1), 3 months (T2) and 6 months (T3) after baseline.
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The outcomes of health services utilization include the total number of unscheduled visits to general out-patient departments, general practitioners (GP), emergency departments, and hospitals, and the total health service attendance.
The information will be relied on the appointment letter and the report from the subjects.
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Baseline assessments (T1), 3 months (T2) and 6 months (T3) after baseline.
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Współpracownicy i badacze
Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.
Współpracownicy
Publikacje i pomocne linki
Osoba odpowiedzialna za wprowadzenie informacji o badaniu dobrowolnie udostępnia te publikacje. Mogą one dotyczyć wszystkiego, co jest związane z badaniem.
Daty zapisu na studia
Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
5 kwietnia 2024
Zakończenie podstawowe (Szacowany)
30 listopada 2026
Ukończenie studiów (Szacowany)
30 listopada 2028
Daty rejestracji na studia
Pierwszy przesłany
29 czerwca 2026
Pierwszy przesłany, który spełnia kryteria kontroli jakości
2 lipca 2026
Pierwszy wysłany (Rzeczywisty)
8 lipca 2026
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
8 lipca 2026
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
2 lipca 2026
Ostatnia weryfikacja
1 czerwca 2026
Więcej informacji
Terminy związane z tym badaniem
Inne numery identyfikacyjne badania
- Z-JNT
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
NIE
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Nie
Bada produkt urządzenia regulowany przez amerykańską FDA
Nie
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .