An Ecological Momentary Assessment Based Program to Support Self-Management for Post-stroke Patients
The goal of this feasibility study is to test whether a new approach that combines real-time symptom tracking (Ecological Momentary Assessment) with machine learning can help people recovering from a stroke to better manage depression, thinking difficulties, and daily functioning. The main questions it aims to answer are: Is this combined approach practical and acceptable for post-stroke survivors? Does the program improve mood, cognitive function, or functional ability to carry out daily…
Conditions studied
Stroke, Post Stroke
About this study
The goal of this feasibility study is to test whether a new approach that combines real-time symptom tracking (Ecological Momentary Assessment) with machine learning can help people recovering from a stroke to better manage depression, thinking difficulties, and daily functioning. The main questions it aims to answer are: Is this combined approach practical and acceptable for post-stroke survivors? Does the program improve mood, cognitive function, or functional ability to carry out daily activities? Participants will: Use a smartphone app called RehabCare Companion for a period of time Answer brief daily surveys about their mood, thoughts, and activities for one week Receive personalized self-care suggestions generated by machine learning based on their responses Complete assessments of depression, cognition, and functioning before and after the program Take part in a group interview to share their experiences
Interventions
- Behavioral: Ecological Momentary Assessment based Self-management Program — The research team collects participants' EMA data (ie., depression, cognitive function, daily activity, and contextual data) from participants for 7-day and analyze the data by machine learning in the first phase, while provide real-time, individualized, self-care messages to the participants via a personalized self-care AI app in the second phase.
Primary outcomes
- Feasibility of the study: acceptance (Immediately after the intervention (T2).)
- Feasibility of the study: adherence (Immediately after the intervention (T2).)
- Feasibility of the study: experience of the participants in using the app (Immediately after the intervention (T2).)
Eligibility information
Study locations
- Queen Elizabeth Hospital, Hong Kong, Hong Kong 999077 Hong Kong
Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-09-27.