Impact of Pharmacist-led Care Navigation Mediated by Digital Health Tools on Hospital Readmissions

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorHospital de Clinicas de Porto Alegre

About this trial

Hospitalizations for Primary Care-Sensitive Conditions (PCSCs) are potentially avoidable hospital admissions that may be prevented when Primary Health Care provides effective and timely care through prevention, early diagnosis, appropriate management of chronic conditions, and control of acute episodes.

This study proposes an open-label, pragmatic, cluster-randomized clinical trial to evaluate the effectiveness of continuous telecare, supported by digital health tools, in the post-discharge follow-up of patients hospitalized for PCSCs.

The main outcome will be the occurrence of non-elective hospital readmissions and urgent or emergency care visits within 180 days after discharge, compared with usual care.

The intervention will include pharmacist-led teleconsultations, a communication channel through a messaging app, and the development of an individualized care plan. Participants in the control group will receive the usual care provided by the healthcare network.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Individuals aged 18 years or older;

Residing in the municipality of Porto Alegre;

Hospitalized at Hospital de Clínicas de Porto Alegre for selected Primary Care-Sensitive Conditions (PCSCs): respiratory diseases (such as asthma, chronic obstructive pulmonary disease, and tuberculosis), cardiovascular diseases (such as arterial hypertension, angina, and heart failure), cerebrovascular diseases (such as stroke), and metabolic diseases (such as diabetes mellitus).

Disqualifiers

Individuals who are unable to be contacted by telephone;

Individuals with language or cognitive barriers that cannot be overcome with the assistance of a caregiver or legal representative;

Individuals participating in another clinical trial that conflicts with the present study.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Pharmacist-led teleconsultations

    Behavioral

    Continuous pharmacist-led care program supported by digital health tools, which will include: three pharmacist teleconsultations, with the first consultation within 15 days after hospital discharge, the second within 30 days, and the third within 90 days; an open communication channel through a messaging app; an individualized care plan; and referrals to other Primary Health Care professionals, when necessary.

Treatment groups

3,220 Participants
are divided into 2 treatment groups
Group A: Pharmacist-led teleconsultationsActive comparator 1 intervention
Group B: Usual careNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Occurrence of non-elective hospital readmissions and visits to urgent and emergency care services within 180 days after hospital discharge

Occurrence of non-elective hospital readmissions and visits to urgent and emergency care services within 180 days after hospital discharge, assessed through patient/caregiver reports during follow-up visits and electronic medical records.

Time frame
From enrollment until 180 days after hospital discharge

Secondary outcomes

1

Proportion of participants who died within 180 days after hospital discharge

Proportion of participants who died within 180 days after hospital discharge, assessed through caregiver reports and medical records.

Time frame
From enrollment until 180 days after hospital discharge
2

Proportion of participants who fully or predominantly completed the actions outlined in the individualized care plan

Proportion of participants who fully or predominantly completed the actions outlined in the individualized care plan, as documented in pharmacist teleconsultations and medical records. An individualized care plan will be developed for each participant based on the Clinical Protocols and Therapeutic Guidelines of the Brazilian Ministry of Health and will include agreed-upon actions. Throughout the follow-up period, completion of the planned actions will be documented. Participants will be considered adherent to the care plan if there is documentation that they completed all planned actions or at least 75% of them within the defined period.

Time frame
From enrollment until 180 days after hospital discharge
3

Satisfaction with continuous pharmacist-led care

Satisfaction with continuous pharmacist-led care will be assessed using the Net Promoter Score (NPS), based on the standard question: "On a scale from 0 to 10, how likely are you to recommend pharmacist-led telecare to a friend or family member?". Respondents will be classified as promoters (score 9-10), passives (score 7-8), or detractors (score 0-6). The NPS will be calculated as the difference between the percentage of promoters and the percentage of detractors, resulting in a score ranging from -100 to +100 (NPS = % Promoters - % Detractors).

Time frame
From enrollment until 180 days after hospital discharge

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Hospital de Clinicas de Porto Alegre

Lead sponsor

Institute of Artificial Intelligence in Health

Collaborator

This trial is not recruiting at the moment. You can still explore other options: