Assessment and Treatment of Chronic Anger and Aggression Following Military-Related Interpersonal and Institutional Betrayal: A Pilot Investigation
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 40
- 试验地点
- 2
- 主要终点
- Successful recruitment
研究概览
简要总结
The goal of this clinical trial is to learn if a treatment designed to deal with anger and aggression from a past betrayal will work. The study will be done on active duty military service members and veterans aged 18 or older. The main questions it aims to answer are:
- Will participants be satisfied with the treatment, and is the treatment feasible to do in a military outpatient setting
- Will the treatment help with anger and aggression issues.
Researchers will compare differences in groups that have different wait times (2-, 3-, or 4-weeks).
Participants will complete surveys before, during and after the treatment. The treatment will be 14 modules given twice a week. About 1 month after treatment ends, surveys will be taken again.
详细描述
Participants will undergo the study procedures described below. The preferred method of assessment and treatment is face-to-face in the STRONG STAR offices at Fort Cavazos. However, there may be circumstances when participants can complete the treatment through telebehavioral health (i.e., by phone or using a HIPAA-compliant video calling platform like Zoom). Decisions will be made on a case-by-case basis as issues arise for individuals (e.g., childcare) and in discussion with the treatment team. If participants do not have internet access they may need to complete assessments in person at the STRONG STAR office or by phone.
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During the wait time:
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Complete a 5-10 minute assessment twice per week (Monday/Thursday or Tuesday/Friday) to assess level of anger, aggression, and interactions with others since last assessment.
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The assigned therapist will call participants once a week for a 10-minute, check-in.
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At the end of participants' assigned wait time, they will complete an assessment of level of anger, aggression, interactions with others, mental, and physical health.
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During treatment:
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Begin treatment within 1 week of last wait time assessment.
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Participate in 7-24 (average 14) one-hour bi-weekly (Monday/Thursday or Tuesday/Friday) CART sessions.
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Prior to each session, participants will complete the same 5-10 minute assessment to assess level of anger, aggression, and interactions with others since last assessment.
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At the final treatment session, participants will be scheduled to complete a 1-month follow-up assessment.
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For follow-up:
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Complete a 1-month follow up assessment between 4-8 weeks after the final treatment session.
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Participants will be sent a link to complete the follow-up assessment.
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Complete the same questionnaires completed at pre-treatment plus an exit interview and a brief satisfaction survey.
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
- None
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Adult active duty military service members and veterans aged 18 or older.
- •Endorses a history of military-related betrayal (on the Modified Moral Injury Questionnaire)
- •Endorses problematic anger in the past month (as evidenced by a score of 12 or above on the Dimensions of Anger Reactions; DAR-5)
- •Engaged in at least 1 self-reported act of aggression in the past 1 month (on the Overt Aggression Scale-Modified; OAS-M)
排除标准
- •Participated in an anger management or trauma-focused intervention within the past 3 months as assessed by self-report.
- •Acute suicidality requiring immediate intervention, such as hospitalization as assessed by the Depressive Symptoms Index-Suicidality Subscale (DSI-SS) combined with follow up clinical interview for elevated scores.
- •Is currently homicidal with plans and intent to hurt a specific person and requiring immediate intervention as measured by self-report and follow-up with clinician if screened positive.
- •Moderate to severe brain injury as measured by inability to comprehend the informed consent document or baseline assessments.
- •Has severe alcohol consumption patterns as evidenced by a score of 19 or above on the Alcohol Use Disorders Identification Test (AUDIT).
- •Experiencing active psychosis or mania as measured by the Prodromal Questionnaire-Brief Version and the Mood Disorders Questionnaire.
结局指标
主要结局
Successful recruitment
时间窗: Study start to last subject enrolled, approximately 1 year
Number of eligible referrals that are recruited, enrolled into the study and randomized to treatment
Client satisfaction survey (CSQ-8)
时间窗: 1 month after study end ( at approximately 11-18 weeks)
The survey will assess participant acceptability using the CSQ-8, an 8-item self-report measure designed to assess client satisfaction. Each question is answered on a 4-point scale with a possible range of scores between 8-32. A higher score indicates a higher level of overall satisfaction. Mean scores will be used to determine participant satisfaction.
Overt Aggression Scale-Modified (OAS-M)
时间窗: Baseline to 1 month post treatment (approximately 11-18 weeks)
A 17-item measure that assesses frequency of different aggression acts in outpatient settings, including verbal and physical aggression against self, other, and objects. The OAS-M is scored by summing the instances of aggression since the last assessment. The OAS-M had been administered as an interview as well as self-report and will be administered as a self-report in this study, consistent with past aggression research with veterans (Miles, Kent et al., 2020). The score is calculated using a sum total of all instances of aggression. Higher scores indicate a greater frequency of aggressive behaviors.
Inventory of Interpersonal Problems-Short Version (IIP-32)
时间窗: Baseline to 1 month post treatment (approximately 11-18 weeks)
A 32-item self-report assessment designed to measure interpersonal functioning. Items are scored on a five-point scale from 0 (not at all) to 4 (extremely) in response to the stem: "How much have you been distressed by this problem?" There are 8 factors and a total score. The 8 factors are: hard to be assertive, hard to be sociable, hard to be supportive, too dependent, too caring, too aggressive, hard to be involved and too open. The possible total score ranges from a T-score are 0-100. T-scores that are higher than 60 are above average and T-scores 70 or higher suggest significant interpersonal difficulty.
State Trait Anger Expression Inventory-2 (STAXI-2)
时间窗: Baseline to 1 month post treatment (approximately 11-18 weeks)
A 57-item inventory which measures the frequency and intensity of anger as an emotional state. There are 6 scales, 5 subscales, and an Anger Expression Index (total anger expression). The State Anger scale (15 items) measures anger intensity as a momentary emotional state, while the Trait Anger scale (10 items) measures the disposition to experience angry feelings as a personality-like trait over lengthy time periods (i.e., the individual's disposition to become angry or angry temperament). The Anger Expression scale (16 items) and the Anger Control scale (16 items) measure four anger-related trait dimensions. Ratings of items are on a 4-point response scales that measure state anger (intensity) as well as trait anger (frequency). The possible total range is a T-score from 0 to 100. Individuals with anger scores higher than the 75-percentile experience and/ or express angry feelings to a degree that may interfere with optimal functioning.
次要结局
- Rate of protocol completion(Treatment end (Approximately 7-14 weeks))
- Number of modules completed(Baseline to end of treatment (approximately 7-14 weeks))
- Brief Inventory of Psychosocial Functioning (B-IPF)(Baseline to 1 month post treatment (approximately 11-18 weeks))
- Dimensions of Anger Reactions (DAR-5)(Baseline to 1 month post treatment (approximately 11-18 weeks))
- Revised Conflict Tactics Scale Short Form (CTS-2)(Baseline to 1 month post treatment (approximately 11-18 weeks))
- Trauma-Related Anger Scale (TRAS)(Baseline to 1 month post treatment (approximately 11-18 weeks))
研究者
Vanessa Jacoby
Associate Professor
The University of Texas Health Science Center at San Antonio
