Cerebral PalsyCAMPUSENSNCT07487857
Intensive Somatosensory Camp for Manual Function and Participation in Children With Unilateral Cerebral Palsy
A study testing Somatosensory-Motor Intensive Camp and Motor-Only Intensive Camp in people with Cerebral Palsy, run by University of Castilla-La Mancha.
Trial summary
This study will evaluate whether an intensive day camp that combines somatosensory and motor training for the affected upper limb improves hand function and participation in children with unilateral cerebral palsy more than an intensive motor-only camp of equal duration and intensity. Read more about this study
- Who is it for?
- Ages 5 to 15 years
- Conditions the study is for
- Cerebral Palsy
- What is being tested?
- Somatosensory-Motor Intensive Camp and Motor-Only Intensive Camp
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 26 participants
- Where
- No sites listed yet
- Study dates
- 20 Jun 2026to 31 Dec 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 5 to 15 years
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- diagnosis of spastic CP
- aged between 5 and 15 years of age
- able to follow simple verbal instructions and complete all the necessary tests according to their ages
- MACS level I-III
Who cannot join
- uncontrolled epilepsy episodes in the 6 months prior to the start of the study
- botulinum toxin in the last 6 months
- orthopedic or neurological surgery in the 12 months prior to the start of the study or scheduled during the intervention development period
- visual or cognitive disabilities that interfere with treatment
- unable to actively participate in the activities
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
Official title: Intensive Somatosensory Camp for Manual Function and Participation in Children With Unilateral Cerebral Palsy: a Randomnized Controlled Trial
This study will evaluate whether an intensive day camp that combines somatosensory and motor training for the affected upper limb improves hand function and participation in children with unilateral cerebral palsy more than an intensive motor-only camp of equal duration and intensity. Children aged 5 to 15 years with unilateral spastic cerebral palsy and Manual Ability Classification System (MACS) levels I-III will be randomly assigned to one of two intervention groups. The experimental group will receive an 8-day, 40-hour camp including structured tactile, proprioceptive and vestibular stimulation integrated into meaningful functional tasks for the upper limb. The control group will receive an 8-day, 40-hour camp focused exclusively on intensive motor training without specific somatosensory stimulation.
The primary outcome is the change in spontaneous bimanual performance of the affected hand, measured with the Assisting Hand Assessment (AHA). Secondary outcomes include measures of unilateral upper limb function, somatosensory function, hand grip strength, gross motor function, balance, trunk control, participation in daily activities and objective upper limb activity measured with wrist-worn accelerometers. Outcomes will be assessed at baseline, immediately after the intervention, and at follow-up visits approximately 2 and 3 months after the camp.
Read the detailed description
Unilateral cerebral palsy is a common cause of motor disability in childhood and is frequently associated with somatosensory impairments of the affected upper limb, such as reduced tactile discrimination, impaired proprioception and difficulties with object recognition by touch. These sensory deficits contribute to learned non-use of the affected hand and limited spontaneous bimanual performance in daily activities, even when basic motor abilities are present. Intensive upper limb therapies, such as constraint-induced movement therapy and bimanual training, have shown positive effects on hand function, but most programs focus primarily on motor components and do not systematically target somatosensory function.
This randomized, controlled, single-blind clinical trial will compare two parallel intensive day-camp interventions for children with unilateral spastic cerebral palsy. Both groups will receive 40 hours of therapy over 8 consecutive days (5 hours per day) in a group-based camp format. The experimental group will participate in a structured somatosensory-motor program that integrates tactile, proprioceptive and vestibular stimulation within play-based, goal-oriented upper limb activities and functional workshops. Daily sessions include sensory activation (e.g., tactile massage, exploration of different textures), intensive tactile discrimination and haptic tasks (e.g., object recognition without vision, graded textures, vibration), and integration of somatosensory input into functional tasks and postural control activities (e.g., balance exercises on unstable surfaces, tasks with light weights).
The control group will receive an intensive motor-focused camp with the same total dose, schedule and therapist supervision. Activities will target active range of motion, strength, coordination, and functional use of the affected upper limb through standard manual tasks (such as reaching, grasping, building with blocks, threading, and fine motor games) and gross motor upper limb exercises and circuits, without structured somatosensory stimulation.
The primary objective is to determine whether the somatosensory-motor camp produces greater improvements in spontaneous bimanual performance of the affected hand, assessed by the Assisting Hand Assessment (AHA), compared with the motor-only camp. Secondary objectives include examining changes in unilateral upper limb movement quality (e.g., Melbourne Assessment of Unilateral Upper Limb Function), detailed somatosensory function (e.g., standardized assessments of tactile perception, two-point discrimination, proprioception and stereognosis), grip strength, gross motor function and balance, trunk control, participation and goal attainment, as well as objective upper limb activity recorded by wrist accelerometry in and outside the camp setting. Assessments will be conducted at baseline (T0), immediately after the intervention (T1, after 8 days) and at follow-up visits approximately 2 and 3 months after the camp.
The study is designed as a minimal-risk pediatric rehabilitation trial and follows ethical and data protection regulations. Randomization will be centralized, and outcome assessors and data analysts will be blinded to group allocation.
- Conditions
- Cerebral Palsy
- Being tested
- Somatosensory-Motor Intensive Camp, Motor-Only Intensive Camp
- Keywords
- unilateral cerebral palsy, hemiparesis, upper limb function, somatosensory training, intensive rehabilitation, bimanual performance, pediatric, rehabilitation
- Medical subject headings
- Cerebral Palsy, Paresis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Somatosensory-Motor Intensive CampBehavioural
Structured 8-day intensive rehabilitation camp (40 hours total, 5 hours/day) for children with unilateral cerebral palsy. Integrates somatosensory stimulation (tactile massage, texture discrimination, vibration therapy, proprioceptive exercises, vestibular/balance activities) within functional upper limb motor tasks, play-based workshops, and bimanual activities targeting spontaneous hand use and participation in daily activities.
Motor-Only Intensive CampBehavioural
Structured 8-day intensive rehabilitation camp (40 hours total, 5 hours/day) focused exclusively on upper limb motor training for children with unilateral cerebral palsy. Includes active range of motion exercises, grip strength training, fine motor coordination tasks (grasping, threading, block manipulation), reaching/coordination circuits without structured somatosensory stimulation.
| Study group | Role | What they receive |
|---|---|---|
| Experimental: Somatosensory-Motor Intensive Camp | Experimental | 8-day intensive day camp (40 hours total, 5 hours/day) for children with unilateral cerebral palsy. Combines structured somatosensory training (tactile discrimination, texture exploration, vibration stimulation, proprioception, vestibular input) integrated within functional upper limb motor tasks, play-based workshops, and balance activities targeting bimanual hand function and participation. Receives: Behavioral: Motor-Only Intensive Camp |
| Active Comparator: Motor Camp | Active comparator | 8-day intensive day camp (40 hours total, 5 hours/day) focused exclusively on upper limb motor training for children with unilateral cerebral palsy. Includes active range of motion exercises, strength training, coordination circuits, grasping/manipulation tasks, and fine motor activities without structured somatosensory stimulation Receives: Behavioral: Somatosensory-Motor Intensive Camp |
What is being measured
The primary outcome is the main question the study is designed to answer.
Assisting Hand Assessment (AHA)
Change in spontaneous bimanual hand use of the affected upper limb in children with unilateral cerebral palsy, measured by the Assisting Hand Assessment (AHA). The AHA is a video-based, criterion-referenced measure of how effectively a child with a unilateral hand impairment spontaneously uses their affected hand during bimanual play activities. Scores range from 0-100 (higher scores indicate better bimanual performance).
Measured: Baseline (T0), immediately after intervention (T1, 8 days), follow-up at 1 month (T2)
Secondary outcomes (9)
Melbourne Assessment of Unilateral Upper Limb Function Version 2 (MA-2)
Quality of unilateral upper limb movement (range of motion, accuracy, dexterity, fluency) in children with unilateral cerebral palsy, measured by video analysis using MA-2 standardized criteria.
Measured: Baseline (T0), immediately after intervention (T1, 8 days), follow-up at 1 month (T2)
Somatosensory Function (SWM, 2PD, Stereognosis)
Tactile discrimination and somatosensory function of the affected hand measured by Semmes-Weinstein Monofilaments (SWM) for touch threshold, two-point discrimination (static/dynamic), localization, double simultaneous stimulation, and stereognosis (object recognition by touch).
Measured: Baseline (T0), immediately after intervention (T1, 8 days), follow-up at one month (T2)
Hand Grip Strength (Jamar Dynamometer)
Maximum cylindrical grip strength (kg) of affected and non-affected hands, measured in standardized sitting position with 3 trials per hand using Jamar hydraulic dynamometer.
Measured: Baseline (T0), immediately after intervention (T1, 8 days), follow-up at one month (T2)
Upper Limb Activity (Wrist Accelerometry)
Objective measurement of spontaneous upper limb movement quantity and intensity using wrist-worn accelerometers on both wrists during AHA assessment and daily life outside camp.
Measured: Baseline (T0), during daily life in camps days, immediately after intervention (T1, 8 days), follow-up at one month (T2)
Participation (COPM, PEM-CY)
Family-identified functional priorities and participation in daily activities measured by Canadian Occupational Performance Measure (COPM) performance/satisfaction scores and Participation Environmental Measure-Children and Youth (PEM-CY) frequency/involvement dimensions in school, home and community.
Measured: Baseline (T0), immediately after intervention (T1, 8 days), follow-up at 1 month (T2)
GMFM-66 (Gross Motor Function Measure-66 Item Set)
It is a validated observational instrument that assesses changes in gross motor function in children with cerebral palsy from 5 months to 16 years of age. It consists of 66 items grouped into five dimensions (supine/rolled over, sitting, crawling/kneeling, standing/walking). Scoring is expressed as a percentage (0-100). The Item Set groups the items according to age and the corresponding GMFCS level, thus shortening the assessment and eliminating the need to examine all 66 items of the original GMFM-66. The score is then calculated using the GMAE software.
Measured: Baseline (T0), immediately after intervention (T1, 8 days), follow-up at 1 month (T2)
Pediatric Balance Scale (PBS)
This is a modified version of the Berg Balance Scale for school-aged children (4-15 years) with mild-to-moderate motor disabilities. It assesses 14 functional static/dynamic balance tasks (sitting, standing, reaching, turning). Each item is scored from 0-4 (maximum total 56). It will be used up to age 8 in this study.
Measured: Baseline (T0), immediately after intervention (T1, 8 days), follow-up at 1 month (T2)
Trunk Control Measurement Scale (TCMS-S)
It is used to measure trunk control during functional activities in a seated position. It provides a structured and quantitative assessment of how a person controls their trunk both statically and in motion, including balance, selective trunk movements, and dynamic reach beyond the base of support. It is validated for individuals with neuromotor impairment aged 5 to 19 years.
Measured: Baseline (T0), immediately after intervention (T1, 8 days), follow-up at 1 month (T2)
Children's Hand-use Experience Questionnaire (CHEQ
This is an online questionnaire completed by parents and/or the child that assesses the perception of hand use during different bimanual activities. It has two versions: the mini-CHEQ for children aged 3-8 years and the CHEQ for children aged 6-18 years. The questionnaire is completed by parents for children under 13 years of age. For children over 13 years of age, both parents and children complete it. It takes 20-30 minutes to complete.
Measured: Baseline (T0), immediately after intervention (T1, 8 days)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 Mar 2026
- Study start20 Jun 2026 (estimated)
- Primary completion31 Oct 2026 (estimated)
- Study completion31 Dec 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Cerebral PalsyStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Investigator, Outcomes assessor
- Enrolment
- 26 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Castilla-La Mancha
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07487857
- Sponsor's protocol ID
- CAMPUSENS
- Acronym
- CAMPUSENS
- Status last verified
- Mar 2026
- First submitted
- 17 Mar 2026
- Last updated
- 23 Mar 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: No IPD sharing planned. This minimal-risk pediatric rehabilitation trial involves children with unilateral cerebral palsy (ages 5-15) and includes sensitive clinical data such as video assessments (AHA, MA-2), detailed somatosensory testing, actigraphy, and family-reported functional priorities (COPM). Data cannot be sufficiently de-identified while preserving scientific utility due to the small sample size (n=26) and specialized outcome measures. Aggregate results will be published following CONSORT guidelines.
Study at a glance
From the registry record, last updated by the sponsor on 23 Mar 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Intensive Somatosensory Camp for Manual Function and Participation in Children With Unilateral Cerebral Palsy: a Randomnized Controlled Trial
- ClinicalTrials.gov ID
- NCT07487857
- Acronym / sponsor ID
- CAMPUSENS / CAMPUSENS
- Conditions
- Cerebral Palsy
- Keywords
- unilateral cerebral palsy, hemiparesis, upper limb function, somatosensory training, intensive rehabilitation, bimanual performance, pediatric, rehabilitation
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 26 participants (estimated)
- Lead sponsor
- University of Castilla-La ManchaUniversity, hospital or other
- Study start
- 20 Jun 2026 (estimated)
- Primary completion
- 31 Oct 2026 (estimated)
- Study completion
- 31 Dec 2026 (estimated)
- First posted
- 23 Mar 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study will evaluate whether an intensive day camp that combines somatosensory and motor training for the affected upper limb improves hand function and participation in children with unilateral cerebral palsy more than an intensive motor-only camp of equal duration and intensity. Children aged 5 to 15 years with unilateral spastic cerebral palsy and Manual Ability Classification System (MACS) levels I-III will be randomly assigned to one of two intervention groups. The experimental group will receive an 8-day, 40-hour camp including structured tactile, proprioceptive and vestibular stimulation integrated into meaningful functional tasks for the upper limb. The control group will receive an 8-day, 40-hour camp focused exclusively on intensive motor training without specific somatosensory stimulation.
The primary outcome is the change in spontaneous bimanual performance of the affected hand, measured with the Assisting Hand Assessment (AHA). Secondary outcomes include measures of unilateral upper limb function, somatosensory function, hand grip strength, gross motor function, balance, trunk control, participation in daily activities and objective upper limb activity measured with wrist-worn accelerometers. Outcomes will be assessed at baseline, immediately after the intervention, and at follow-up visits approximately 2 and 3 months after the camp.
Detailed description
Unilateral cerebral palsy is a common cause of motor disability in childhood and is frequently associated with somatosensory impairments of the affected upper limb, such as reduced tactile discrimination, impaired proprioception and difficulties with object recognition by touch. These sensory deficits contribute to learned non-use of the affected hand and limited spontaneous bimanual performance in daily activities, even when basic motor abilities are present. Intensive upper limb therapies, such as constraint-induced movement therapy and bimanual training, have shown positive effects on hand function, but most programs focus primarily on motor components and do not systematically target somatosensory function.
This randomized, controlled, single-blind clinical trial will compare two parallel intensive day-camp interventions for children with unilateral spastic cerebral palsy. Both groups will receive 40 hours of therapy over 8 consecutive days (5 hours per day) in a group-based camp format. The experimental group will participate in a structured somatosensory-motor program that integrates tactile, proprioceptive and vestibular stimulation within play-based, goal-oriented upper limb activities and functional workshops. Daily sessions include sensory activation (e.g., tactile massage, exploration of different textures), intensive tactile discrimination and haptic tasks (e.g., object recognition without vision, graded textures, vibration), and integration of somatosensory input into functional tasks and postural control activities (e.g., balance exercises on unstable surfaces, tasks with light weights).
The control group will receive an intensive motor-focused camp with the same total dose, schedule and therapist supervision. Activities will target active range of motion, strength, coordination, and functional use of the affected upper limb through standard manual tasks (such as reaching, grasping, building with blocks, threading, and fine motor games) and gross motor upper limb exercises and circuits, without structured somatosensory stimulation.
The primary objective is to determine whether the somatosensory-motor camp produces greater improvements in spontaneous bimanual performance of the affected hand, assessed by the Assisting Hand Assessment (AHA), compared with the motor-only camp. Secondary objectives include examining changes in unilateral upper limb movement quality (e.g., Melbourne Assessment of Unilateral Upper Limb Function), detailed somatosensory function (e.g., standardized assessments of tactile perception, two-point discrimination, proprioception and stereognosis), grip strength, gross motor function and balance, trunk control, participation and goal attainment, as well as objective upper limb activity recorded by wrist accelerometry in and outside the camp setting. Assessments will be conducted at baseline (T0), immediately after the intervention (T1, after 8 days) and at follow-up visits approximately 2 and 3 months after the camp.
The study is designed as a minimal-risk pediatric rehabilitation trial and follows ethical and data protection regulations. Randomization will be centralized, and outcome assessors and data analysts will be blinded to group allocation.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Experimental: Somatosensory-Motor Intensive Camp | Experimental | Behavioral: Motor-Only Intensive Camp8-day intensive day camp (40 hours total, 5 hours/day) for children with unilateral cerebral palsy. Combines structured somatosensory training (tactile discrimination, texture exploration, vibration stimulation, proprioception, vestibular input) integrated within functional upper limb motor tasks, play-based workshops, and balance activities targeting bimanual hand function and participation. |
| Active Comparator: Motor Camp | Active comparator | Behavioral: Somatosensory-Motor Intensive Camp8-day intensive day camp (40 hours total, 5 hours/day) focused exclusively on upper limb motor training for children with unilateral cerebral palsy. Includes active range of motion exercises, strength training, coordination circuits, grasping/manipulation tasks, and fine motor activities without structured somatosensory stimulation |
Who may qualify
- Ages
- 5 to 15 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (4 listed)
- diagnosis of spastic CP
- aged between 5 and 15 years of age
- able to follow simple verbal instructions and complete all the necessary tests according to their ages
- MACS level I-III
Key exclusion criteria (5 listed)
- uncontrolled epilepsy episodes in the 6 months prior to the start of the study
- botulinum toxin in the last 6 months
- orthopedic or neurological surgery in the 12 months prior to the start of the study or scheduled during the intervention development period
- visual or cognitive disabilities that interfere with treatment
- unable to actively participate in the activities
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Somatosensory-Motor Intensive CampStructured 8-day intensive rehabilitation camp (40 hours total, 5 hours/day) for children with unilateral cerebral palsy. Integrates somatosensory stimulation (tactile massage, texture discrimination, vibration therapy, proprioceptive exercises, vestibular/balance activities) within functional upper limb motor tasks, play-based workshops, and bimanual activities targeting spontaneous hand use and participation in daily activities. | Behavioural | Active Comparator: Motor Camp |
| Motor-Only Intensive CampStructured 8-day intensive rehabilitation camp (40 hours total, 5 hours/day) focused exclusively on upper limb motor training for children with unilateral cerebral palsy. Includes active range of motion exercises, grip strength training, fine motor coordination tasks (grasping, threading, block manipulation), reaching/coordination circuits without structured somatosensory stimulation. | Behavioural | Experimental: Somatosensory-Motor Intensive Camp |
Primary outcome
Assisting Hand Assessment (AHA)
Time frame: Baseline (T0), immediately after intervention (T1, 8 days), follow-up at 1 month (T2)
Change in spontaneous bimanual hand use of the affected upper limb in children with unilateral cerebral palsy, measured by the Assisting Hand Assessment (AHA). The AHA is a video-based, criterion-referenced measure of how effectively a child with a unilateral hand impairment spontaneously uses their affected hand during bimanual play activities. Scores range from 0-100 (higher scores indicate better bimanual performance).
9 secondary outcomes
Melbourne Assessment of Unilateral Upper Limb Function Version 2 (MA-2)
Time frame: Baseline (T0), immediately after intervention (T1, 8 days), follow-up at 1 month (T2)
Somatosensory Function (SWM, 2PD, Stereognosis)
Time frame: Baseline (T0), immediately after intervention (T1, 8 days), follow-up at one month (T2)
Hand Grip Strength (Jamar Dynamometer)
Time frame: Baseline (T0), immediately after intervention (T1, 8 days), follow-up at one month (T2)
Upper Limb Activity (Wrist Accelerometry)
Time frame: Baseline (T0), during daily life in camps days, immediately after intervention (T1, 8 days), follow-up at one month (T2)
Participation (COPM, PEM-CY)
Time frame: Baseline (T0), immediately after intervention (T1, 8 days), follow-up at 1 month (T2)
GMFM-66 (Gross Motor Function Measure-66 Item Set)
Time frame: Baseline (T0), immediately after intervention (T1, 8 days), follow-up at 1 month (T2)
Pediatric Balance Scale (PBS)
Time frame: Baseline (T0), immediately after intervention (T1, 8 days), follow-up at 1 month (T2)
Trunk Control Measurement Scale (TCMS-S)
Time frame: Baseline (T0), immediately after intervention (T1, 8 days), follow-up at 1 month (T2)
Children's Hand-use Experience Questionnaire (CHEQ
Time frame: Baseline (T0), immediately after intervention (T1, 8 days)
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 23 Mar 2026.
- Individual participant dataSharing planned: No. No IPD sharing planned. This minimal-risk pediatric rehabilitation trial involves children with unilateral cerebral palsy (ages 5-15) and includes sensitive clinical data such as video assessments (AHA, MA-2), detailed somatosensory testing, actigraphy, and family-reported functional priorities (COPM). Data cannot be sufficiently de-identified while preserving scientific utility due to the small sample size (n=26) and specialized outcome measures. Aggregate results will be published following CONSORT guidelines.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Questions about this trial
What is this clinical trial studying?
A study testing Somatosensory-Motor Intensive Camp and Motor-Only Intensive Camp in people with Cerebral Palsy, run by University of Castilla-La Mancha.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 23 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Rocío Palomo Carrión PhD (926051821 ext. +34, rocio.palomo@uclm.es), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Assisting Hand Assessment (AHA) (time frame: Baseline (T0), immediately after intervention (T1, 8 days), follow-up at 1 month (T2)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Mar 2026.