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Four-week Open-trial Extension TNS for ADHD

Primary Purpose

Attention Deficit Hyperactivity Disorder (ADHD)

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Active TNS
Sponsored by
University of California, Los Angeles
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Attention Deficit Hyperactivity Disorder (ADHD) focused on measuring ADHD, neuromodulation, trigeminal nerve stimulation

Eligibility Criteria

8 Years - 12 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • male and female children ages 8-12 with DSM-5 ADHD, and current presentation, as determined by KSADS and clinical interview
  • participated in a previous randomized, double-blind, sham-controlled trial of TNS for ADHD, and randomized to the sham condition.
  • parents able and willing to monitor proper use of the TNS device and complete all required rating scales
  • parent and participants able to compete study rating scales and other measures in English

Exclusion Criteria:

  • currently requiring any medication with CNS effects

Sites / Locations

  • UCLA Semel Institute

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Active TNS

Arm Description

Participants who previously underwent screening and determination of eligibility in a double-blind sham-controlled trial of TNS for ADHD, and randomized to sham, will be offered upon unblinding at the end of the 5-week controlled trial to receive 4-weeks open treatment with the active TNS condition.

Outcomes

Primary Outcome Measures

ADHD-IV Rating Scale (ADHD-RS)
A dimensional rating of ADHD symptoms, with scores ranging from 0 to 54, with higher scores signifying worse severity.

Secondary Outcome Measures

Clinical Global Impression - Improvement (CGI-I)
Categorical measure indicating degree improved or not improved compared with global functioning at baseline in the preceding double-blind trial. The base CGI-I scale is a 7-point measure that requires the investigator to assess how much the condition has improved or worsened compared to baseline prior to initiation of treatment. Ratings are (1) very much improved; (2) much improved; (3) minimally improved; (4) no change; (5) minimally worse; (6) much worse; (7) very much worse. For purposes of analysis, the measure is dichotomized such that scores <= 2 signify "improved" and scores > 2 signify "not improved."
Height
A dimensional measure assessed in cm.
Weight
A dimensional measure assessed in kg.
Systolic Blood Pressure
A dimensional measure assessed in mm HG.
Diastolic Blood Pressure
A dimensional measure assessed in mm HG.
Pulse
A dimensional measure assessed in heart beats per minute.

Full Information

First Posted
March 5, 2019
Last Updated
May 17, 2019
Sponsor
University of California, Los Angeles
Collaborators
National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT03870737
Brief Title
Four-week Open-trial Extension TNS for ADHD
Official Title
Four-week Open-trial Extension Study of Trigeminal Nerve Stimulation (TNS) for Youth Previously Randomized to Sham in a Double-Blind Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2019
Overall Recruitment Status
Completed
Study Start Date
December 1, 2014 (Actual)
Primary Completion Date
May 30, 2018 (Actual)
Study Completion Date
May 30, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, Los Angeles
Collaborators
National Institute of Mental Health (NIMH)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Device Product Not Approved or Cleared by U.S. FDA
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study will be to offer children previously randomized to sham treatment in a 5-week double-blind sham controlled study of Trigeminal Nerve Stimulation for ADHD (NCT02155608) an opportunity to receive 4-weeks active TNS treatment.
Detailed Description
This study will enroll participants with ADHD who previously participated in a 5-week sham-controlled investigation of Trigeminal Nerve Stimulation as a treatment for ADHD, and who were randomized to the sham condition. In the double-blind trial (NCT02155608), children ages 8-12 years undergo study screening and if eligible begin 4 weeks nightly treatment with active or sham TNS administered nightly during sleep. At the conclusion of the 4-week trial, all interventions (both active and sham TNS) are discontinued with blinding remaining in place for an additional week to assess possible residual treatment effects. Participants' randomized condition is unblinded at Week 5. All participants randomized to sham in the double-blind trial are invited to participate in a 4-week open-trial of TNS to allow all participants the opportunity to benefit from the active intervention. During this 4-week open-extension trial, interested participants will receive nightly active TNS during sleep. The final study visit (Visit 5) of the double-blind study will serve as baseline for this open-extension. Participants will return for clinic assessments at Weeks 2 and 4. Participants who achieve clinically significant improvement from active TNS over the 4-week open trial will be invited to receive a year of nightly active-TNS therapy as part of a 12-month extension study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Attention Deficit Hyperactivity Disorder (ADHD)
Keywords
ADHD, neuromodulation, trigeminal nerve stimulation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
22 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Active TNS
Arm Type
Experimental
Arm Description
Participants who previously underwent screening and determination of eligibility in a double-blind sham-controlled trial of TNS for ADHD, and randomized to sham, will be offered upon unblinding at the end of the 5-week controlled trial to receive 4-weeks open treatment with the active TNS condition.
Intervention Type
Device
Intervention Name(s)
Active TNS
Other Intervention Name(s)
Trigeminal Nerve Stimulation, Monarch eTNS SystemTM (NeuroSigma, Inc., Los Angeles CA
Intervention Description
Participants will receive 4-weeks nightly treatment with active TNS. Positive responders will be invited to participate in 12-month open-extension study.
Primary Outcome Measure Information:
Title
ADHD-IV Rating Scale (ADHD-RS)
Description
A dimensional rating of ADHD symptoms, with scores ranging from 0 to 54, with higher scores signifying worse severity.
Time Frame
Change over Baseline, Week 2, Week 4.
Secondary Outcome Measure Information:
Title
Clinical Global Impression - Improvement (CGI-I)
Description
Categorical measure indicating degree improved or not improved compared with global functioning at baseline in the preceding double-blind trial. The base CGI-I scale is a 7-point measure that requires the investigator to assess how much the condition has improved or worsened compared to baseline prior to initiation of treatment. Ratings are (1) very much improved; (2) much improved; (3) minimally improved; (4) no change; (5) minimally worse; (6) much worse; (7) very much worse. For purposes of analysis, the measure is dichotomized such that scores <= 2 signify "improved" and scores > 2 signify "not improved."
Time Frame
Change over Baseline, Week 2, Week 4
Title
Height
Description
A dimensional measure assessed in cm.
Time Frame
Change over Baseline, Week 2, Week 4
Title
Weight
Description
A dimensional measure assessed in kg.
Time Frame
Change over Baseline, Week 2, Week 4
Title
Systolic Blood Pressure
Description
A dimensional measure assessed in mm HG.
Time Frame
Change over Baseline, Week 2, Week 4
Title
Diastolic Blood Pressure
Description
A dimensional measure assessed in mm HG.
Time Frame
Change over Baseline, Week 2, Week 4
Title
Pulse
Description
A dimensional measure assessed in heart beats per minute.
Time Frame
Change over Baseline, Week 2, Week 4
Other Pre-specified Outcome Measures:
Title
Conners Global Index - Parent Report
Description
Parent completed dimensional rating of ADHD symptoms,with score range from 0- 30, and higher scores indicating more severe symptoms.
Time Frame
Change over Baseline and weekly for 4-week trial
Title
Conners Global Index - Teacher Report
Description
Teacher completed dimensional rating of ADHD symptoms,with scores ranging from 0-30, and higher scores indicating more severe symptoms.
Time Frame
Change over Baseline and weekly for 4-week trial
Title
Affective Reactivity Index (ARI-C) Child
Description
A child-completed dimensional measure of emotional reactivity,with scores ranging from 0-12, and higher scores indicating greater severity.
Time Frame
Change over Baseline, Week 4
Title
Affective Reactivity Index (ARI-P) Parent
Description
A parent-completed dimensional measure of emotional reactivity, with scores ranging from 0-12, and higher scores indicating greater severity.
Time Frame
Change over Baseline, Week 4
Title
Children's Sleep Habits Questionnaire (CSHQ)
Description
A parent-completed 33-item scale to assess sleep related problems. Total scores range from 33 to 99 divided among 8 sub scales , with higher scores indicating more severe difficulties.
Time Frame
Change over Baseline and weekly for 4-week trial
Title
Multidimensional Anxiety Scale for Children (MASC) - Child Report
Description
A child-completed rating of child anxiety, with scores ranging from 0-300, and higher scores indicating greater severity.
Time Frame
Change over Baseline and Week 4
Title
Multidimensional Anxiety Scale for Children (MASC) - Parent Report
Description
A parent-completed rating of child anxiety, with scores ranging from 0-300, and higher scores indicating greater severity.
Time Frame
Change over Baseline and Week 4
Title
Children's Depression Rating Scale - Revised (CDRS-R)
Description
A clinician-completed dimensional measure of childhood mood symptoms obtained from parent and child interview, with range of scores from 17 to 113, and higher scores indicating more severe depression. A score >= 40 suggests depression; scores <= 28 defines remission.
Time Frame
Change over Baseline and Week 4
Title
Behavior Rating Inventor of Executive Functioning (BRIEF)
Description
A parent completed rating of child executive function. Comprises 5 sub scales that measure various measures of behavior and cognition. Raw scores on each measure are converted to T scores ranging from 28 to 103, with higher scores indicating greater difficulties.
Time Frame
Change over Baseline and weekly during 4-week trial
Title
Columbia-Suicide Severity Rating Scale (C-SSRS)
Description
standard instrument to assess potential suicidality with dichotomous scores (0 = absent; 1 = present) to rate various components of suicidal ideation and behavior. Data derived are summarized under Adverse Event Reporting.
Time Frame
Baseline and weekly during 4-week trial

10. Eligibility

Sex
All
Minimum Age & Unit of Time
8 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: male and female children ages 8-12 with DSM-5 ADHD, and current presentation, as determined by KSADS and clinical interview participated in a previous randomized, double-blind, sham-controlled trial of TNS for ADHD, and randomized to the sham condition. parents able and willing to monitor proper use of the TNS device and complete all required rating scales parent and participants able to compete study rating scales and other measures in English Exclusion Criteria: currently requiring any medication with CNS effects
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
James J. McGough, M.D.
Organizational Affiliation
University of California, Los Angeles
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sandra K. Loo, Ph.D.
Organizational Affiliation
University of California, Los Angeles
Official's Role
Principal Investigator
Facility Information:
Facility Name
UCLA Semel Institute
City
Los Angeles
State/Province
California
ZIP/Postal Code
90095
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Four-week Open-trial Extension TNS for ADHD

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