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临床试验/NCT06144203
NCT06144203招募中不适用

The Influence of Aerobic Exercise on Consolidation of Fear Extinction Learning in PTSD

University of Alabama, Tuscaloosa2 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2024年1月29日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
120
试验地点
2
主要终点
Skin conductance responses

研究概览

简要总结

This study aims to test whether aerobic exercise performed after fear extinction learning improves cognitive, physiological, and neural indices of extinction recall in a sample of trauma-exposed men and women with and without posttraumatic stress disorder (PTSD). Participants will complete a clinical intake visit (Day 0), followed by a three-day fear conditioning (day 1), fear extinction + activity (day 2), and fear extinction recall (day 3) protocol.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 64 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • male or female sex
  • right-handed
  • age 18-64
  • a current diagnosis of PTSD where the index event involves interpersonal violence exposure (e.g., physical/sexual assault).
  • Inclusion criteria for the trauma-exposed (without PTSD) control participants includes:
  • male or female sex
  • right-handed
  • age 18-64
  • interpersonal violence exposure (e.g., physical/sexual assault).

排除标准

  • for all participants:
  • current substance use disorder (other than alcohol, nicotine, or cannabis)
  • acute suicidality
  • history of bipolar/psychotic disorder
  • changes to or addition of psychiatric medication in the past 4 weeks (6 weeks for fluoxetine)
  • medications that effect neurovascular properties upon which BOLD fMRI capitalizes (e.g., water pills)
  • history of neurological disorders or disease (e.g., traumatic brain injury, epilepsy, seizures)
  • loss of consciousness > 10 minutes
  • intellectual disabilities (IQ<70)
  • developmental disorders
  • MRI contraindication (e.g., internal ferromagnetic objects such as electronic devices, surgical implants, shrapnel; see phone screen)
  • claustrophobia or the inability to lie still in a confined space
  • physical disabilities that prohibit task performance (e.g., blindness or deafness)
  • positive pregnancy test
  • cochlear implant
  • an implanted neurostimulator
  • physical disabilities that prohibit task performance (e.g., blindness or deafness)
  • vulnerable populations (i.e., pregnant women, individuals appearing to lack consent capacity, prisoners, individuals unable to read consent materials, individuals in a relationship with study researchers (e.g., friends, family members, significant others)
  • having a history of chest pain during physical activity
  • having a bone, joint, cardiac, or other medical condition that a doctor has said may be worsened by physical activity
  • having asthma
  • responding 'Yes' to any of the seven questions on the Physical Activity Readiness Questionnaire (PAR-Q - administered as part of the Exercise Safety Questions of the phone screen), indicating it is unsafe for the individual to engage in aerobic exercise without physician approval (i.e., potential participant would be eligible to participate if they indicated 'Yes' to one or more of the PAR-Q items provided they obtain a doctor's note indicating it is safe for them to participate in the study)
  • Percutaneous Coronary Intervention or acute myocardial infarction in the last 6 weeks
  • unstable arrhythmias/implanted cardiac defibrillator shocks in the last 3 months
  • any other condition that the PI believes might put the participant at risk.
  • Additionally, due to their effects on image quality, interested individuals with the following may be ineligible to participate per PI's judgement: nonremovable dental implants (e.g., braces or upper permanent retainers) as these will distort the MRI images we collect (note: filings, crowns, and silver or gold teeth are okay); any other condition, medication, or implant that the PI believes would degrade image quality or render data unusable

结局指标

主要结局

Skin conductance responses

时间窗: Collected during fear conditioning, fear extinction, and extinction recall task.

SCR data will be collected while participants are completing the cognitive task in the MRI environment.

Threat expectancy ratings

时间窗: Collected during fear conditioning, fear extinction, and extinction recall task.

Threat expectancy ratings will be collected while participants are completing the cognitive task in the MRI environment.

Neural activity

时间窗: Collected during fear conditioning, fear extinction, and extinction recall task.

Neural activity will be collected while participants are completing the cognitive task in the MRI environment.

次要结局

未报告次要终点

研究者

发起方
University of Alabama, Tuscaloosa
申办方类型
Other
责任方
Principal Investigator
主要研究者

Kevin Crombie

Assistant Professor

University of Alabama, Tuscaloosa

研究点 (2)

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