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临床试验/NCT06080373
NCT06080373尚未招募不适用

Formulation-Based Cognitive-Behavioral Therapy Compared to an Active Control and a Waitlist in Adult Inmates With ADHD: A Randomized Controlled Trial

Universidad Europea de Valencia0 个研究点目标入组 111 人开始时间: 2027年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
111
主要终点
Conners Adult ADHD Diagnostic Interview for DSM-IV (CAADID)

研究概览

简要总结

Background Recent literature suggests that ADHD is a risk factor for the development of antisocial behavior that is more severe and persistent than in community and other psychiatric populations. The combination of stimulant medication and psychotherapy (particularly cognitive-behavioral therapy, CBT) is considered an evidence-based intervention for adults with ADHD. In contrast, few studies have evaluated the efficacy of medication in adult prisoners with ADHD, and the literature on the efficacy of psychotherapy is virtually nonexistent. Therefore, this article presents the protocol of a trial that will assess the efficacy of a formulation-based CBT program for inmates with ADHD.

Methods The study has a multicenter randomized controlled trial design. After screening and recruitment, participants will be randomly assigned to the CBT intervention, a general offender treatment program, or a waitlist. Pre- and post-treatment self-report and clinician-report assessments, as well as 6- and 12-month follow-up assessments will be conducted. These will include both clinical (e.g., ADHD symptoms, depression and anxiety symptoms, self-esteem, alcohol/drug abuse, treatment adherence, quality of life) and criminological (e.g., recidivism and risk of recidivism) measures. Linear mixed models will be used to assess differences between groups.

Discussion This study may be the first to evaluate the efficacy of a psychotherapy intervention in adult inmates with ADHD. It is expected that addressing the specific needs of ADHD would not only result in the previously reported clinical improvements (e.g., reduction in ADHD and comorbidity symptoms), but also reduce the risk and rate of recidivism compared to the general intervention or no intervention. However, the design may be limited by the difficulties inherent in the prison setting and in following up the sample after release.

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
Single (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

入选标准

  • To have signed written informed consent to participate in the study
  • To be between 18 and 65 years of age
  • To meet the DSM-5 diagnostic criteria for ADHD (American Psychiatric Association, 2013)
  • To have been convicted of at least one crime under Spanish or German criminal law
  • To have been incarcerated for at least six months and three or fewer years since the completion of the conviction at the time of eligibility assessment.

排除标准

  • To have a severe personality disorder, psychotic disorder, or pervasive developmental disorder as their primary diagnosis, as the intervention would not meet their clinical needs
  • To have an IQ of 80 or less, as measured by a standardized IQ test (Raven et al., 1993), due to the complexity of the cognitive components in the CBT program
  • To have participated in a previous psychological intervention for ADHD;
  • To not be fluent in Spanish or German, depending on the study site.

研究组 & 干预措施

Formulated-based cognitive behavioral therapy

Experimental

Participants randomized to the CBT group will receive a minimum of 13 and a maximum of 22 sessions of individual formulation-based CBT. It will be delivered by psychologists trained in CBT, according to a manual that will be available soon. Prior to intervention, a behavioral assessment is conducted to operationalize each case's clinically relevant behaviors, antecedents, and maintenance stimuli. Each case will be formulated and presented to the participant in simple and easy to understand language. To illustrate this, a schematic formulation of the typical case of an adult with ADHD is shown in Figure 2. Specific behavioral goals will then be agreed upon for each participant. To achieve these goals, various treatment strategies will be presented in the following sessions. The choice of strategies, the order in which they are applied, and the duration of each module will be customized for each participant according to the case formulation.

干预措施: Formulation-based cognitive behavioral therapy (Behavioral)

PROBECO and social therapeutic establishments

Active Comparator

The Spanish participants assigned to the active control group will receive the PROBECO. It is a group program designed by the Spanish Penitentiary Agency for its application with inmates convicted of different types of violent crimes . Its main goals are to eradicate criminal behavior and reduce recidivism, to modify the relevant dynamic risk factors related to general delinquency, and to introduce new social skills and prosocial values. It consists of four phases: (I) general intervention: aimed at the acquisition of social skills; (II) specific intervention: consists of four specific educational itineraries; (III) relapse prevention; (IV) follow-up.

Similarly, German participants will be assigned to a special type of prison known as a social therapeutic facility, where they will undergo compulsory psychotherapy focused primarily on relapse prevention.

干预措施: PROBECO (Behavioral)

Waitlist

No Intervention

Participants in waitlist control group will receive no treatment while experimental groups are treated. They will be offered to receive CBT after the study.

结局指标

主要结局

Conners Adult ADHD Diagnostic Interview for DSM-IV (CAADID)

时间窗: Pre and post-treatment plus follow-up assessments 6 and 12 months after the end of the intervention

This is considered one of the primary outcomes. The CAADID is a structured interview divided into two parts. Part I may be self-administered or clinician-administered and collects information on the subject's demographic history, developmental history, associated risk factors, and comorbidity, while Part II must be administered by a trained clinician and assesses DSM-IV criteria for ADHD in adults. Only Part II will be used for the study, as information on patient history is not relevant for measuring response to interventions.

Reoffending rate

时间窗: Pre and post-treatment plus follow-up assessments 6 and 12 months after the end of the intervention

This will be the primary criminological outcome. Police records will be checked every 6 months after the end of treatment to look for new arrests. We will also try to check court and prison records for new convictions and incarcerations. However, access to this information may be very limited in European criminal justice systems, so it may be difficult to obtain.

次要结局

  • Maudsley Addiction Profile (MAP)(Pre and post-treatment plus follow-up assessments 6 and 12 months after the end of the intervention)
  • Beck depression inventory-II (BDI-II) and Beck anxiety inventory (BAI)(Pre and post-treatment plus follow-up assessments 6 and 12 months after the end of the intervention)
  • Clinical Global Impression (CGI)(Pre and post-treatment plus follow-up assessments 6 and 12 months after the end of the intervention)
  • Attention-deficit/hyperactivity rating scale-IV(Pre and post-treatment plus follow-up assessments 6 and 12 months after the end of the intervention)
  • Rosenberg self-esteem scale (RSES(Pre and post-treatment plus follow-up assessments 6 and 12 months after the end of the intervention)
  • Adult ADHD Quality of Life Questionnaire (AAQoL(Pre and post-treatment plus follow-up assessments 6 and 12 months after the end of the intervention)
  • Historical Clinical Risk Management-20 (HCR-20)(Pre and post-treatment plus follow-up assessments 6 and 12 months after the end of the intervention)

研究者

发起方
Universidad Europea de Valencia
申办方类型
Other
责任方
Principal Investigator
主要研究者

Carlos López-Pinar

Proffesor

Universidad Europea de Valencia

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