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NCT07691411Recruiting

An Ecological Momentary Assessment Based Program to Support Self-Management for Post-stroke Patients

Combining Machine Learning and Ecological Momentary Assessment of Depression, Cognitive Function and Daily Activity Behavior to Support Self-Management for Post-stroke Patients: A Feasibility Study

Source: ClinicalTrials.gov · Last updated 8 Jul 2026

Brief summary (registry, in English)

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

Status (registry)
Recruiting
Study type
Interventional
Enrollment
50 (estimated)
First submitted
29 Jun 2026
Start date
6 Jan 2026
Primary completion date
30 Sept 2026
Lead sponsor
The Hong Kong Polytechnic University
Diseases
Stroke
NCT number
NCT07691411

What you commit to

  • Study type: Interventional
  • Planned participants: 50
  • From 6 Jan 2026 to the primary completion date, 30 Sept 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • they have moderate to severe cognitive impairment (a HK-MoCA score of 17 or lower)
  • they have active psychiatric disorders other than depression (e.g., schizophrenia, bipolar disorder)
  • they have a terminal illness or prognosis that suggests a limited life expectancy
  • they have conditions that compromise their self-care ability (i.e., bedbound).

Who the study is looking for

  • adults aged 18 years or older
  • having a confirmed diagnosis of stroke
  • having sufficient proficiency in Cantonese to understand and respond to the assessments and prompts
  • having a Hong Kong version of the Montreal Cognitive Assessment (HK-MoCA) score of 18 or higher
  • having a smartphone.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Queen Elizabeth Hospital
Coordinator of this site? Confirm its status
Hong KongHong Kong SAR ChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.