Nurse-Led Discharge Program and Primary Care Outcomes: A Proof-of-concept Cluster Randomized Controlled Trial

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorThe University of Hong Kong

About this trial

The goal of this cluster randomized controlled trial is to evaluate whether a nurse-led primary health care (PHC) discharge intervention can improve patient activation and primary health care-related outcomes among hospitalized adult patients after discharge.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Hong Kong residents aged ≥18 years

Able to read and communicate in Chinese (Cantonese or Mandarin)

Being hospitalized for more than 24 hours

Stable medical condition upon hospital discharge

Disqualifiers

Having a history of psychiatric/psychological disease or currently on regular psychotropic medications

Currently participating in other primary healthcare programmes

Trial design

Design model

Parallel

Treatments tested in this trial

  • Primary healthcare discharge education

    Behavioral

    The primary healthcare discharge education begins by identifying priorities to address related to patients' life situations (using the Instrument for Patient Capacity Assessment) and determining the patient's current level of activation (using the Patient Activation Measure). A discharge education guide developed by the research team helps to individualize the teaching according to the patient's priorities and activation level.

  • specially-designed health education leaflet

    Behavioral

    1. Introduction of the District Health Centres/Expresses; 2. Life Course Preventive Care Plan pamphlet; 3. Provide disease-specific discharge/rehabilitation advice and relevant health education materials with an emphasis on prevention and self-care management; 4. The hospital nurses will help discharge patients download and install the "HA Go" mobile app.

  • Patient discharge package

    Behavioral

    Subjects in the intervention group will receive the following items with instructions for use upon hospital discharge: 1. Blood pressure monitor 2. Blood glucose test strip 3. Soft ruler to measure weight circumference 4. Resistance bands for simple exercise

  • usual hospital discharge practice

    Behavioral

    The control group will receive the usual hospital discharge practice upon discharge.

Treatment groups

120 Participants
are divided into 2 treatment groups
Group A: Intervention groupExperimental treatment 3 interventions
Group B: Control GroupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

The primary outcome is the change in the Patient Activation Measure (PAM) between baseline and 3-month follow-up.

The PAM is a 13-item self-report questionnaire to measure patient activation level \[18\]. Patients can go through four levels of activation: (1) disengaged and overwhelmed, (2) becoming aware but still struggling, (3) taking action, and (4) maintaining behaviors and pushing further \[18\].PAM raw score can be calculated by adding all of the responses to the 13 questions \[18\]. This score is then converted into an activation score ranging from 0 = no activation to 100 = high activation using a scoresheet provided by Insignia Health.

Time frame
From baseline to 3-month follow up.

Secondary outcomes

Other outcomes

Sponsors and contacts

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The University of Hong Kong

Lead sponsor

Queen Mary Hospital, Hong Kong

Collaborator

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