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RECRUITING NA

Operant Conditioning of the Soleus Stretch Reflex in Adults With Cerebral Palsy

NCT05571033 · View on ClinicalTrials.gov ↗

Study Summary

12 adults with spastic CP will complete 6 baseline sessions and 24 down conditioning sessions held 3 times/week. All clinical and physiological assessments collected at baseline will be reassessed after study completion, and follow ups after 2 weeks, 1 month and 3 months. The soleus H reflex (electric analogue of the stretch reflex) will be elicited in all sessions. In each session, participants will complete 20 baseline trials and 225 down conditioning trials to decrease the magnitude of the H-Reflex.

Interventions

  • BEHAVIORAL Spinal reflex conditioning

Study Locations (1)

New York

  • Burke Neurological Institute — White Plains

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2022-09-30
Est. Completion 2026-12-31
Phase NA

Sponsor

Burke Medical Research Institute

5 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05571033

The ClinicalTrials.gov registry entry for NCT05571033 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 12 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Burke Medical Research Institute, which has 5 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Cerebral Palsy appearing as the primary indexed condition, and to 1 intervention — of which Spinal reflex conditioning is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05571033 reports 1 study location spanning 1 distinct geographic area — top geographies include New York. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05571033 about?

NCT05571033 is a clinical study titled "Operant Conditioning of the Soleus Stretch Reflex in Adults With Cerebral Palsy". 12 adults with spastic CP will complete 6 baseline sessions and 24 down conditioning sessions held 3 times/week. All clinical and physiological assessments collected at baseline will be reassessed after study completion, and follow ups after 2 weeks, 1 month and 3 months. The soleus H reflex (electr...

What is the current status of trial NCT05571033?

This trial is currently recruiting. It is a NA study. The enrollment target is 12 participants. The study started on 2022-09-30. Estimated completion is 2026-12-31.

What conditions does trial NCT05571033 study?

This clinical trial studies the following conditions: Cerebral Palsy, Spastic Cerebral Palsy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05571033?

The interventions under investigation include: Spinal reflex conditioning (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05571033?

This trial is sponsored by Burke Medical Research Institute, which has 5 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05571033 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial