NCT06190795Completed
A Smartphone Application for a Self-directed Upper Limb Therapy After Stroke
Feasibility and Effectiveness of AI-powered Interactive Smartphone Application for a Self-directed Upper Limb Therapy Implementation After Stroke
Source: ClinicalTrials.gov · Last updated 10 Sept 2025
Brief summary (registry, in English)
The aim of study is to investigate a newly developed AI smartphone application's feasibility, usefulness in improving users' experience, effect on adherence, UL use and recovery after stroke. The study is a prospective randomized controlled trial (RCT) to compare the implementation of AMPLIFY, a self-directed UL programme for people with stroke in two modes of delivery- hardcopy manual versus the mobile application. Eighty people with stroke within 4 weeks of stroke will be randomly allocated to either the experimental group (smartphone app) or control group (hardcopy manual) to undergone four weeks of AMPLIFY program. To compare the clinical effects of delivery AMPLIFY program via smartphone app versus hardcopy manual, assessments will be done at three time points- pre-intervention, post-intervention and three months post-intervention.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 38 (actual)
- First submitted
- 19 Dec 2023
- Start date
- 11 Mar 2024
- Primary completion date
- 31 Mar 2025
- Lead sponsor
- Tan Tock Seng Hospital
- Diseases
- Stroke
- NCT number
- NCT06190795
What you commit to
- Study type: Interventional
- Participants enrolled: 38
- From 11 Mar 2024 to the primary completion date, 31 Mar 2025
- 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.
Prior treatment
- Reduced paretic upper limb use prior to stroke episode (e.g. frozen shoulder, fracture, etc)
Other illness
- Bilateral stroke
- Reduced paretic upper limb use due to orthopaedic problems such as fracture in existing stroke episode
- Severe behavioural disturbance or agitation or epilepsy or untreated depression or psychiatric conditions
Other
- Montreal Cognitive Assessment (MOCA)\<21
- Paretic upper limb numeric pain rating scale (NPRS)\>5
- Medically unstable
- Neglect as ascertained by treatment team
- Pregnancy or lactation states
Who the study is looking for
- Diagnosis of stroke (confirmed by CT/MRI scans)
- ≤four weeks post-stroke
- Montreal Cognitive Assessment (MOCA)\>=21
- Finger extension Medical Research Council (MRC) \>=1
- Fugl Meyer Upper Limb score \<60 or NIHSS Motor Arm section score\>=2
- Potential discharge to home (able to do tele-rehabilitation for review)
Age in the registry: 21 years to 90 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Lay Fong Chin Coordinator of this site? Confirm its status | Singapore | Singapore | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.