- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07664631
Effects of Stimulant Medications in PTSD (SMP)
2026년 6월 18일 업데이트: University of Chicago
While there have been advances in understanding post-traumatic stress disorder (PTSD) as a disorder and its biological features, unfortunately only one out of five traumatized persons with PTSD reach remission after cycling through evidence-based and/or FDA-approved medications.
This is especially unfortunate given that people with PTSD are often from vulnerable populations, or those whose professions entail personal sacrifice.
It is clear that new serotonergic antidepressants and atypical antipsychotics will not be sufficient to fix this gap, and new mechanisms of action need to be tested.
In the current proposal, the investigators test the hypothesis that mixed amphetamine salts (brand name Adderall), FDA-approved for treating attention deficit hyperactivity disorder (ADHD), can improve PTSD outcomes.
연구 개요
상세 설명
Post-traumatic stress disorder is a debilitating neuropsychiatric condition triggered by exposure to a traumatic exposure.
Approximately 8% of the US population will experience the condition in their lifetime.
At-risk populations, such as those exposed to community violence or warfare, have nearly double the risk.
Despite progress in recognizing that PTSD is a disorder of neural circuits that underlie how individuals learn from the world, available treatments, including two FDA-approved medications (serotonergic antidepressants) and gold-standard evidence-based psychotherapies, help only one in five individuals reach remission.
One key aspect of PTSD is difficulty in engaging in social interactions.
Based on surprising evidence published in peer-reviewed manuscripts from our research programs at The University of Chicago, medications used to treat ADHD have positive effects on social interaction.
Combined with promising data from biological studies of PTSD, psychostimulants used to safely treat ADHD such as Adderall (generic: mixed amphetamine salts), can help people with PTSD re-engage in social relationships that are the key to their recovery.
This study will test the hypothesis that mixed amphetamine salts will acutely increase social interaction in adults with PTSD compared to placebo in a novel laboratory-based social interaction task.
연구 유형
중재적
등록 (추정된)
40
단계
- 1단계
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 연락처
- 이름: Hanna Molla
- 전화번호: 7737023560
- 이메일: hmolla@uchicago.edu
연구 장소
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Illinois
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Chicago, Illinois, 미국, 60637
- University of Chicago
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연락하다:
- Hanna Molla
- 전화번호: 7737023560
- 이메일: hmolla@uchicago.edu
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수석 연구원:
- Royce Lee
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참여기준
연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
예
설명
Inclusion Criteria:
- Age 18 - 65 years old
- BMI 19-30 kg/m2
- English fluency
Exclusion Criteria:
- Individuals with current moderate or severe substance use disorder, no past stimulant or cocaine use disorder
- Individuals with current acute or high risk of suicide or suicide attempt in past 6 months
- Individuals with current psychotic or bipolar disorder
- Individuals with past schizophrenia, schizoaffective disorder, psychotic bipolar disorder, stimulant or cocaine use disorder
- Individuals with chronic (non-PRN) treatment with antipsychotic drug (except PRN quetiapine 25mg PO qHS) or D2 antagonist
- Individuals with medications with significant PD or PK interactions
- Individuals with current treatment with a stimulant medication
- Individuals with court or legally mandated treatment
- Individuals with unstable or untreated medical disorder that would increase the risk of serious side effects of study drug (unstable hypertension, tachycardia, cardiac arrhythmia, recent MI or stroke, clinically significant neuropsychiatric or neurological disorder)
- Members of a vulnerable population
- High blood pressure (>140/90)
- Women who are pregnant, breastfeeding, or planning to become pregnant
공부 계획
이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 크로스오버 할당
- 마스킹: 더블
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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위약 비교기: placebo
dextrose
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dextrose
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실험적: Adderall
Adderall (20 mg)
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mixed amphetamine salts
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Quality of Social Interaction Ratings using the Conversation Questionnaire
기간: Completed 4 hours post-drug administration during both sessions (drug, placebo)
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6 items on a 9 point Likert scale.
Higher scores indicate increased quality of social interactions
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Completed 4 hours post-drug administration during both sessions (drug, placebo)
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Quality of Social Interaction Ratings using connection during conversation scale
기간: Completed 4 hours post-drug administration during both sessions (drug, placebo)
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9 point Likert scale with 16 items.
Includes subscales: conversation enjoyment, perceived meaningfulness, and feelings of interpersonal connection.
Higher scores indicate increased quality of social interactions
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Completed 4 hours post-drug administration during both sessions (drug, placebo)
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공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
간행물 및 유용한 링크
연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.
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연구 기록 날짜
이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.
연구 주요 날짜
연구 시작 (추정된)
2026년 9월 15일
기본 완료 (추정된)
2027년 9월 15일
연구 완료 (추정된)
2027년 9월 15일
연구 등록 날짜
최초 제출
2026년 6월 15일
QC 기준을 충족하는 최초 제출
2026년 6월 18일
처음 게시됨 (실제)
2026년 6월 24일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
2026년 6월 24일
QC 기준을 충족하는 마지막 업데이트 제출
2026년 6월 18일
마지막으로 확인됨
2026년 6월 1일
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- IRB25-1935
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
미정
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
예
미국 FDA 규제 기기 제품 연구
아니
미국에서 제조되어 미국에서 수출되는 제품
예
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .