ClinicalTrials.gg
Active, not recruitingNCT05753345Updated Jun 30, 2026

Aquatic Therapy for Children With Neuromotor Deficits

An interventional study of Aquatic therapy in Cerebral Palsy and Hypoxia, Brain, sponsored by Ohio State University. Active, not recruiting at 1 site in United States. Open to participants aged 3 Years to 9 Years. Per ClinicalTrials.gov, last updated 2026-06-30.

Sponsored by Ohio State University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
36
Allocation
Not applicable
Ages
3 Years to 9 Years
Sex
All
01

Study summary

The purpose of this study is to explore the feasibility, fidelity and acceptability of an aquatic therapy assessment and intervention for children ages 3-9 with neuromotor deficits such as cerebral palsy. The intervention takes place in a warm water therapy pool, twice a week for ten weeks and targets swim safety skills, upper extremity function and self care participation and performance.

Read the detailed description

The purpose of this study is to explore the feasibility, fidelity and acceptability of an aquatic therapy assessment and intervention. The intervention will target swim safety skills, upper extremity function and self care participation and performance in children with neuromotor conditions such as cerebral palsy. The study includes an intake evaluation session, twenty sessions of aquatic therapy (twice a week for 10 weeks) and a post evaluation session. This takes place in Columbus, Ohio.

Each session will be a combination of land-based self care training and water-based upper extremity exercise and swim skill training. The intervention structure will include the following:

  1. Self Care Session: Doffing clothing, preparing for swimming
  2. Motor learning aquatic activities guided by individualized goals
  3. Self Care session: Towel dry, rinse off, dressing

Individualized activities will be planned according to the individualized goals written for each child participant.

02

Conditions studied

  • Cerebral Palsy
  • Hypoxia, Brain
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

Ohio State University is the lead sponsor of 663 studies on the registry; 148 are open to participants now.

Of its 67 completed or terminated interventional studies of FDA-regulated products, 49 (73%) have results posted.

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

04

Who can participate

Ages eligible
3 Years to 9 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

  • 3-9 years for the children, 18+ for the parents/guardians.
  • child with neuro-motor diagnosis (CP, hypoxia, etc.)
  • child impairments in upper extremity function
  • child deficits in performance of self care activities

Exclusion criteria

Exclusion Criteria:

  • compromised airway
  • uncontrolled seizures
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
36 participants (estimated)

Study arms

  • Experimental
    Intervention: aquatic occupational therapy (AquOTic-NM)

    aquatic occupational therapy 30 minutes, self care training 15 minutes

    Behavioral: Aquatic therapy

Interventions

  • BehavioralAquatic therapy

    Children receive aquatic occupational therapy twice a week for 10 weeks. 30 minutes of aquatic therapy in a warm water pool to increase upper extremity function and swim skills; 15 minutes of self care training to increase independence with dressing and showering.

06

What researchers measure

Primary outcomes

  1. Change in Water Orientation Test Alyn (WOTA)

    performance based swim skill assessment

    Time frame: Baseline, immediately after the intervention

  2. Change in Pediatric Evaluation of Disability Index, Computer Adaptive Text (PEDI-CAT)

    parent reported questionnaire regarding child's self care skills

    Time frame: baseline, immediately after the intervention

  3. Change in Quality of Upper Extremity Skills Test (QUEST)

    performance-based assessment of upper extremity skills

    Time frame: baseline, immediately after intervention

Secondary outcomes

  1. Change in Participation and Environment Measure (PEM-CY)

    parent reported questionnaire of participation in home, school and community

    Time frame: baseline, immediately after the intervention

  2. Change in Canadian Occupational Performance Measure (COPM)

    Parent perception of goals attained

    Time frame: baseline, immediately after the intervention

07

Study locations

1 site
  • Erika Kemp
    Columbus, Ohio 43210, United States
08

References and documents

Individual participant data

Plan to share: No — Deidentified data may be shared with researchers upon request

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jan 2023 (actual). Primary completion is estimated for Dec 2026, 47 months after the start.

Of 902 non-industry interventional studies with no phase under Cerebral Palsy, half reached primary completion within 12 months of starting (the median), counting those still running; a quarter within 5 and three quarters within 31. This study's planned 47 months is above that.

Counting every sponsor, half of 921 studies reached it within 12 months; a quarter within 5 and three quarters within 31.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 3, 2023
First posted
Mar 3, 2023
StartActual
Jan 9, 2023
Primary completionEst.
Dec 30, 2026
CompletionEst.
Dec 30, 2026
Last update
Jun 30, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jun 30, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05753345
Collaborators
Franklin County Board of Developmental Disabilities
Responsible party
Erika Kemp (Assistant Professor, Clinical, Ohio State University) — Principal investigator
First posted
Mar 3, 2023
Start date
Jan 9, 2023
Primary completion
Dec 30, 2026 (estimated)
Completion
Dec 30, 2026 (estimated)
Last update
Jun 30, 2026

Oversight

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

Not currently enrolling

This study is active, not recruiting, as verified in Jun 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