Clinical and Electrographic Changes in Responsive Neurostimulation System (RNS) Patients with Acupuncture Treatment

Part of paid clinical trials in Houston, Texas.

Sponsor
The University of Texas Health Science Center, Houston
Study ID
NCT04677751
Status
Recruiting

Conditions

Eligibility Criteria

Sex
ALL
Age
15 Years - 60 Years
Healthy Volunteers
Not accepted

Interventions

  • Acupuncture intervention — DEVICE
    Participants will undergo 12 weeks of acupuncture therapy. There will be one 40 minute-1 hour. session per week.

Study Details

The purpose of this study is to determine effects of Acupuncture on a Patient's mood and cognition,evaluate changes in clinically-reported seizure frequency and severity and analyze effects of Acupuncture on electrographic epileptiform activity stored by the RNS System

Key Dates

Start date
Apr 1, 2021
Status verified
Jul 2024
Primary completion
Dec 1, 2025
Completion
Dec 1, 2025

Study Design

Enrollment
10 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE

Arms

  • Experimental: Experimental group

Primary Outcome Measure

Percent change in number of disabling clinical seizures [ Time Frame: Baseline,12 weeks post treatment ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
The University of Texas Health Science Center at HoustonHoustonTexas77030
Olga Rodziyevska, MS,PA-C
(713) 500-5482
Ardonia N Tousant
(713) 500-5482

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