Low-Intensity Focused Ultrasound for Gambling Disorder
A Randomized, Sham-Controlled Trial of Low Intensity Focused Ultrasound Neuromodulation as an Adjunctive Treatment for Gambling Disorder
The goal of this clinical trial is to learn whether low-intensity focused ultrasound (LIFU) is safe and may help reduce gambling-related symptoms in adults seeking treatment for gambling disorder.
The main questions it aims to answer are:
- Is LIFU safe and well tolerated in adults with gambling disorder?
- Does LIFU reduce gambling behavior compared with a sham (inactive) procedure?
Researchers will compare participants who receive active LIFU with participants who receive sham LIFU to see whether active treatment leads to greater reductions in gambling behavior.
Participants will:
- Be randomly assigned to receive either active LIFU or sham LIFU.
- Receive nine treatment sessions delivered over three treatment days within a five-day period.
- Participate in weekly telehealth cognitive behavioral therapy (CBT).
- Complete assessments of gambling behavior, gambling urges, mood, and quality of life.
- Attend follow-up visits for up to 90 days after active LIFU treatment.
Low-intensity focused ultrasound is a noninvasive technique that uses focused sound waves to influence brain activity. Researchers believe this approach may affect brain circuits involved in reward, cravings, and decision-making that contribute to gambling disorder.
研究概览
地位
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习地点
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Virginia
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Charlottesville、Virginia、美国、22903
- University of Virginia
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接触:
- James Mahoney, PhD
- 电话号码:434-924-2097
- 邮箱:jamesmahoney@virginia.edu
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接触:
- Daisy Thompson-Lake, PhD
- 电话号码:434-924-2097
- 邮箱:daisythompsonlake@virginia.edu
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Adults 18 to 60 years old.
- Currently diagnosed with gambling disorder, confirmed by a clinical interview.
- Seeking treatment for gambling disorder, including people currently participating in or transitioning from addiction treatment programs.
- In generally good enough physical health to safely participate in study procedures.
- Not pregnant and not planning to become pregnant during study participation.
- Able to speak and read English well enough to provide informed consent and complete study assessments.
- Able to safely undergo MRI scans (for example, no metal implants or other conditions that would make MRI unsafe).
- Willing to be randomly assigned to either study group, attend all study visits, and participate in weekly telehealth counseling sessions.
Exclusion Criteria:
- Significant heart, lung, liver, kidney, blood vessel, or blood-clotting problems that may make participation unsafe.
- Unwilling to avoid illegal substance use on study procedure days.
- Currently participating in court-ordered treatment.
- Skin or scalp conditions over the treatment area that may interfere with the study procedure.
- A medical condition that the study doctor believes could increase the risks of the ultrasound procedure, such as a history of seizures, stroke, serious brain injury, or certain brain abnormalities.
- Current or past schizophrenia, another psychotic disorder, or bipolar disorder.
- Diagnosis of a Cluster A or Cluster B personality disorder.
- Unable to safely undergo an MRI scan.
- Pregnant or planning to become pregnant during the study.
- Previous treatment with focused ultrasound neuromodulation or another investigational neuromodulation treatment within the past 90 days.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:交叉作业
- 屏蔽:双倍的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:Active LIFU Treatment
Device: Low Intensity Focused Ultrasound
|
Active low-intensity focused ultrasound (LIFU) neuromodulation targeting the left and right nucleus accumbens. Each treatment course comprises three 10-minute sessions per day (5 minutes to the left nucleus accumbens and 5 minutes to the right nucleus accumbens) delivered on three treatment days within a 5-day window, for a total of nine sessions. Participants also receive standard-of-care, once-weekly telehealth cognitive behavioral therapy (CBT). |
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假比较器:Sham LIFU Treatment
Device: Low Intensity Focused Ultrasound
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Sham low-intensity focused ultrasound procedures that are identical to active treatment except that no therapeutic ultrasound energy is delivered. Each treatment course comprises three 10-minute sessions per day on three treatment days within a 5-day window, for a total of nine sessions. Participants also receive standard-of-care, once-weekly telehealth cognitive behavioral therapy (CBT). After completion of the Day 30 primary endpoint assessments and unblinding, participants may cross over to receive open-label active LIFU. |
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Incidence of Device-Related and Procedure-Related Adverse Events
大体时间:Randomization through Day 30
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Number of participants who experience at least one device-related or investigational procedure-related adverse event (AE) or serious adverse event (SAE) during the randomized treatment phase. Adverse event severity and relationship to study procedures will be assessed by the study investigator. |
Randomization through Day 30
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Change From Baseline in Gambling Frequency Measured by the Gambling Timeline Follow-Back (G-TLFB)
大体时间:Baseline to Day 30
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The G-TLFB is a calendar-based self-report assessment that uses memory cues and a timeline method to estimate gambling activity over a specified period. Gambling frequency is assessed by retrospectively recording gambling behavior during the assessment period. Higher values indicate greater gambling frequency. |
Baseline to Day 30
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Change From Baseline in Time Spent Gambling Measured by the Gambling Timeline Follow-Back (G-TLFB)
大体时间:Baseline through Day 90 post-active LIFU treatment
|
The G-TLFB is a calendar-based self-report assessment that retrospectively records gambling behavior over a specified period. The outcome is the total time spent gambling during the assessment period. Higher values indicate greater time spent gambling. |
Baseline through Day 90 post-active LIFU treatment
|
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Change From Baseline in Amount of Money Gambled Measured by the Gambling Timeline Follow-Back (G-TLFB)
大体时间:Baseline through Day 90 post-active LIFU treatment
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The G-TLFB is a calendar-based self-report assessment that retrospectively records gambling behavior over a specified period. The outcome is the total amount of money gambled during the assessment period. Higher values indicate greater gambling expenditure. |
Baseline through Day 90 post-active LIFU treatment
|
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Change From Baseline in Desire to Gamble During a Cue Reactivity Task
大体时间:Baseline through Day 90 post-active LIFU treatment
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Participants will view gambling-related cues and rate their desire to gamble using a visual analog scale ranging from 0 to 100, where 0 indicates no desire to gamble and 100 indicates the strongest desire possible. Higher scores indicate greater desire to gamble. |
Baseline through Day 90 post-active LIFU treatment
|
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Change From Baseline in Gambling Symptom Severity Measured by the Gambling Symptom Assessment Scale (GSAS)
大体时间:Baseline through Day 90 post-active LIFU treatment
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The Gambling Symptom Assessment Scale GSAS is a 12-item self-report measure of gambling urges, thoughts, and behaviors during the previous week. Total scores range from 0 to 48, with higher scores indicating greater gambling symptom severity. |
Baseline through Day 90 post-active LIFU treatment
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Change From Baseline in Gambling Symptom Severity Measured by the Pathological Gambling Yale-Brown Obsessive Compulsive Scale (PG-YBOCS)
大体时间:Baseline through Day 90 post-active LIFU treatment
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The Pathological Gambling Yale-Brown Obsessive Compulsive Scale (PG-YBOCS) is a clinician-administered measure of gambling-related thoughts, urges, and behaviors. Total scores range from 0 to 40, with higher scores indicating greater gambling symptom severity. |
Baseline through Day 90 post-active LIFU treatment
|
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Change From Baseline in Depression Symptom Severity Measured by the Patient Health Questionnaire-9 (PHQ-9)
大体时间:Baseline through Day 90 post-active LIFU treatment
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The Patient Health Questionnaire-9 (PHQ-9) is a 9-item self-report measure of depressive symptoms. Total scores range from 0 to 27, with higher scores indicating greater depression symptom severity. |
Baseline through Day 90 post-active LIFU treatment
|
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Change From Baseline in Anxiety Symptom Severity Measured by the Generalized Anxiety Disorder-7 (GAD-7)
大体时间:Baseline through Day 90 post-active LIFU treatment
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The Generalized Anxiety Disorder-7 (GAD-7) is a 7-item self-report measure of anxiety symptoms. Total scores range from 0 to 21, with higher scores indicating greater anxiety symptom severity. |
Baseline through Day 90 post-active LIFU treatment
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Change From Baseline in Quality of Life Measured by the World Health Organization Quality of Life-BREF (WHOQOL-BREF)
大体时间:Baseline through Day 90 post-active LIFU treatment
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The World Health Organization Quality of Life-BREF (WHOQOL-BREF) is a 26-item self-report measure that assesses physical, psychological, social, and environmental domains of quality of life. Higher scores indicate better quality of life. |
Baseline through Day 90 post-active LIFU treatment
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合作者和调查者
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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