跳至主要内容
临床试验/NCT03648476
NCT03648476已完成不适用

Intervention to Change Attributions That Are Negative (ICAN): a New Approach to Reducing Anger and Aggression After Brain Injury

Indiana University1 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2018年11月2日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
28
试验地点
1
主要终点
Change in Buss-Perry Aggression Questionnaire Score

研究概览

简要总结

ICAN is the first treatment to target hostile attributions after TBI, making it a novel anger/ aggression management approach in this population. This is a randomized waitlist control trial. The length of time in the trial is approximately 15 weeks and the intervention is 6 weeks long.

详细描述

ICAN is the first treatment to target hostile attributions after TBI, making it a novel anger/ aggression management approach in this population. Since the investigator's prior research shows that stronger hostile attributions are associated with poorer perspective taking,39 ICAN employs a unique perspective-positioning technique to train perspective taking and reduce hostile attributions. After recalling a personal situation in which others' ambiguous actions led to an unpleasant outcome, participants will explore different perspectives: sitting or standing in one position, s/he will explore his or her own thoughts and feelings (self-perspective), then move to a different position to experience the other person's perspective, eliciting their thoughts and feelings.

In 40 participants with TBI, we will conduct a Phase I, randomized waitlist controlled trial with 4 data collection points: Baseline; Week 1; Week 8 (post-treatment for ICAN; post-wait period for WLC); Week 15 (WLC post-treatment).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •History of complicated mild to severe TBI (injury due to an external physical force), with injury severity being defined either by Glasgow Coma Score at time of injury (≤12), or post-traumatic amnesia (≥1 day), or loss of consciousness (≥30 minutes), or positive head CT scan consistent with TBI.
  • •At least 18 years of age or older;
  • •≥1 year post-injury;
  • •Have adequate vision, hearing, and speech/ language skills to participate in assessments and group therapy (determined based on interaction with the participant at screening)
  • •Have adequate reading comprehension (due to the primary assessment involving written scenarios)
  • •Have abnormal scores of negative attributions or perspective taking (determined at T0 screening)
  • •Have above average aggression (prescreened on telephone, and confirmed T0 screening).
  • •No anticipated medication changes for emotions/ behavior during length of study participation; medications for emotions/ behavior must be stable within last 30 days prior to consent at T0 (Screening)
  • •Have reliable mode of transportation

排除标准

  • •Pre-morbid neurological disorders that could affect mood and cognition (e.g. stroke); does not include controlled seizures
  • •Progressive central nervous system disorders (e.g. dementia, Parkinson's)
  • •Developmental disability (e.g., autism, developmental delay);
  • •Major psychiatric disorders (e.g. schizophrenia, Borderline Personality Disorder);
  • •Severe Depression and/or perceived risk to self or others (mental health resources will be provided and if suicide risk, approved suicide protocol will be utilized);
  • •Currently receiving active behavioral therapy for anger.
  • •On drug research study for irritability, anger, aggression

研究组 & 干预措施

ICAN

Experimental

6-week group therapy intervention with clinical RA comprised of 6 90-120 minute sessions beginning after Time 1 testing

干预措施: ICAN (Behavioral)

WLC: Waitlist Control

Other

WLC participants will delay treatment until after time two testing 8-weeks from time one testing. Participants will then begin 6 90-120 minute therapy sessions.

干预措施: ICAN (Behavioral)

结局指标

主要结局

Change in Buss-Perry Aggression Questionnaire Score

时间窗: Change from Baseline at Week 8 and Week 15

The Buss-Perry Aggression Questionnaire (AQ), is a standardized measure comprised of 34 statements to assess total aggression, as well as the following aggression subconstructs: anger, hostile thoughts, and physical and verbal aggression. Participants rate statements using a 5-point Likert scale (1, 2, 3, 4, 5). Subscales are summed to compute a Total Aggression raw score and total Aggressions Scores were then converted to T scores (1-100) with a mean T-score =50 and Standard deviation=10 points. Higher T-scores= more aggression/ worse outcome, thus a lower number indicates improvement Here, we are reporting the CHANGE in the group's MEAN t-score (e.g. Mean Post-test T score of 62 MINUS Mean Pre-test t score of 58 = Mean CHANGE score of -4, which means less aggression post-treatment). Thus, we are NOT reporting t-scores in this Results section; just the mean change of these scores. Negative scores indicate an improvement.

次要结局

  • Global Impression of Change for Anger and Aggression(Week 8 for participants randomized to ICAN or Week 15 for those randomized to WLC (administered after receiving treatment))
  • Global Impression of Change for Perspective Taking and Empathy(Week 8 for participants randomized to ICAN or Week 15 for those randomized to WLC (administered after received treatment))
  • Change in Anger Affect Score(Change from Week 1 at Week 8 and Week 15)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dawn Neumann

Principal Investigator

Indiana University

研究点 (1)

Loading locations...

相似试验