ClinicalTrials.gg
Not yet recruitingNCT07041944HEMImprove-APPUpdated Mar 18, 2026

HEMImprove 1.0 in Children and Adolescents With Unilateral Cerebral Palsy

An interventional study of HEMImprove APP and exercises to upper limb in Unilateral Cerebral Palsy, sponsored by University of Castilla-La Mancha. Not yet recruiting. Open to participants aged 12 Years to 18 Years. Per ClinicalTrials.gov, last updated 2026-03-18.

Sponsored by University of Castilla-La Mancha · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
36
Allocation
Randomized
Ages
12 Years to 18 Years
Sex
All
01

Study summary

This study aims to evaluate the effectiveness and usability of HEMImprove 1.0, a gamified mobile application designed to improve upper limb motor function in adolescents with unilateral cerebral palsy. Participants will be randomly assigned to an intervention group using the app or a control group performing conventional home exercises. The intervention will last four weeks, with assessments before and after the intervention to measure motor function, motivation, and quality of life improvements.

02

Conditions studied

  • Unilateral Cerebral Palsy

Browse trials for

03

In context

Cerebral Palsy

1,936 studies on the registry are indexed under Cerebral Palsy; 458 are open to participants now.

This study's planned enrollment of 36 is close to the median of 34 across 1,431 interventional studies indexed under Cerebral Palsy.

Browse Cerebral Palsy studies →

Lead sponsor

University of Castilla-La Mancha is the lead sponsor of 107 studies on the registry; 26 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
12 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adolescents aged 12 to 18 years diagnosed with unilateral cerebral palsy.
  • Ability to use the mobile app independently or with minimal assistance.
  • provided.

Exclusion criteria

Exclusion Criteria:

  • Severe cognitive impairment.
  • Recent upper limb surgery (within 6 months).
  • Recent botulinum toxin treatment (within 3 months).
  • Other neurological or orthopedic disorders affecting upper limb function.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
36 participants (estimated)

Study arms

  • Experimental
    HEMImprove APP

    Experimental Group: Use HEMImprove 1.0 mobile app at home for 30 minutes/session, 5 days/week, for 4 weeks. Exercises tailored progressively with avatar guidance. Control Group: Perform conventional home exercises guided by printed manual with instructions and images, matching frequency and duration of intervention group.

    Other: HEMImprove APP

  • Active comparator
    Control group

    The control group will do exercises for the same time that is described in the experimental group, without using the APP

    Other: exercises to upper limb

Interventions

  • OtherHEMImprove APP

    Experimental Group: Use HEMImprove 1.0 mobile app at home for 30 minutes/session, 5 days/week, for 4 weeks. Exercises tailored progressively with avatar guidance. Control Group: Perform conventional home exercises guided by printed manual with instructions and images, matching frequency and duration of intervention group.

  • Otherexercises to upper limb

    The patients will do the same exercises than the experimental group, without APP and using the same dosage

06

What researchers measure

Primary outcomes

  1. Assisting Hand Assessment

    Time frame: baseline, immediately after the intervention, 3 months after intervention

  2. Melbourne Assessment v 2.0 MA2

    Time frame: baseline, immediately after the intervention, 3 months after intervention

  3. Nine hole Test

    Time frame: baseline, immediately after the intervention, 3 months after intervention

Secondary outcomes

  1. User satisfaction and usability measured through structured Likert-scale questionnaires post-intervention.

    Time frame: From the recruitment to the follow-up

  2. Qualitative data from semi-structured interviews analyzing user experience.

    Time frame: from the recruitment to the end of the treatment

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07041944
Responsible party
Sponsor
First posted
Jun 27, 2025
Start date
Mar 1, 2026 (estimated)
Primary completion
Feb 1, 2027 (estimated)
Completion
Dec 1, 2027 (estimated)
Last update
Mar 18, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Mar 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion