WhatsApp therapy could boost stroke hand recovery
NCT ID NCT07666906
First seen Jun 27, 2026 · Last updated Jul 17, 2026 · Updated 2 times
Summary
This study tests whether adding home-based telerehabilitation via WhatsApp video calls to standard outpatient therapy improves hand function in people who had a stroke 1-6 months ago. Forty-eight participants will be split into two groups: one gets standard therapy plus daily 30-minute video sessions with a physiotherapist, the other gets standard therapy alone. After 6 weeks, researchers will measure changes in arm movement and dexterity.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- telerehabilitation via WhatsApp video calls
- What this could lead to
- If it works, this could offer a convenient, low-cost way to boost hand recovery for stroke patients at home.
- What could go wrong
- This is a small, early-stage trial with only 48 participants, so results may not apply to everyone. The intervention relies on smartphone access and internet, which may limit use.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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48 people
The number who actually took part.
- Started
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Jan 2026
- Expected to finish
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Jul 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 60 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Subacute stroke patients (time since stroke: 1-6 months)\\n * Fugl-Meyer Assessment for Upper Extremity score between 22-56\\n * Box and Block Test score of at least 1 block in 60 seconds at the Screening Visit\\n * Ability to provide informed consent\\n * Access to a smartphone with WhatsApp capability (for Group A) Exclusion Criteria: * Any other major existing neurological or psychotic disease (e.g., Parkinson's disease, multiple sclerosis)\\n * Pregnancy\\n * Any disease apart from index stroke that noticeably affects arm function of paretic limb\\n * Cognitive impairment that prevents understanding of instructions\\n * Upper extremity acute orthopedic conditions\\n * Medically unstable patients
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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The University of Faisalabad
Faisalābad, Punjab Province, 3800, Pakistan
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Other studies related to the condition(s) this trial covers.
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