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临床试验/NCT07247955
NCT07247955已完成不适用

Effectiveness of the Guided and Traditional Cognitive Behavioral Therapy Protocol in a Patient With Treatment-resistant Panic Disorder

Universidade Federal do Rio de Janeiro1 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2023年4月5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
46
试验地点
1
主要终点
Efficacy criteria

研究概览

简要总结

Self-guided therapy for anxiety disorders has focused on various cognitive-behavioral treatments mediated by technologies such as web applications. This study aims to compare two groups of patients with panic disorder undergoing two clinical psychological treatment models: one traditional cognitive behavioral therapy (CBT), and the other self-guided CBT using a digital application.

An application was developed in which both treatment models follow the same eight-session CBT manual. Patients are evaluated using psychological assessments at the first and eighth sessions.

The study includes 46 patients divided into two groups of 23 participants each. Both groups undergo individual assessments at the beginning and end of the treatment protocol.

详细描述

As such, an application was developed whereby the two models follow the same treatment manual of eight sessions, with the patients being evaluated using psychological tests at the first and eighth sessions.

Methods: A total of 46 patients were separated into two groups of 23 patients, one in each format, with the patients in both groups being individually evaluated at their first and eighth sessions.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Patients undergoing IPUB screening through the panic and respiratory laboratory outpatient clinic.
  • •Diagnosis of panic disorder confirmed.
  • •Age between 18 and 60 years.
  • •Under psychiatric follow-up by a university psychiatrist and taking medication.
  • •Provide written informed consent to participate and have data stored.

排除标准

  • •Patients without a diagnosis of panic disorder.
  • •Age under 18 or over 60 years.
  • •Not undergoing psychiatric follow-up.
  • •Presence of other psychiatric or medical diagnoses.

研究组 & 干预措施

Group of 23 patients undergoing traditional cognitive behavioral therapy

Experimental

Twenty-three patients were selected for group. The group consisted of patients with panic disorder and breathing difficulties in a traditional cognitive behavioral therapy format, 8-session treatment protocol.

干预措施: The group intervention used the sessions described in traditional form (Behavioral)

Group of 23 patients undergoing self-guided cognitive behavioral therapy using an app

Experimental

Twenty-three patients were selected for group. The group consisted of patients with panic disorder and breathing difficulties in a self-guided cognitive behavioral therapy format, using the 8-session treatment protocol.

干预措施: The group intervention used the sessions described in a self-guided format using an application (Behavioral)

结局指标

主要结局

Efficacy criteria

时间窗: Baseline (Week 1) and Post-intervention (Week 8)

Primary Outcome Measure 1 Title: Beck Anxiety Inventory (BAI) total score Time Frame: Baseline (Week 1) and Post-intervention (Week 8) Description: The BAI is a 21-item self-report questionnaire that measures the severity of anxiety symptoms. Total scores range from 0 to 63; higher scores indicate greater anxiety. Administered to all participants in both groups. Results will be reported separately for each time point. Unit of Measure: Points on a scale (0-63) Primary Outcome Measure 2 Title: Beck Depression Inventory (BDI) total score Time Frame: Baseline (Week 1) and Post-intervention (Week 8) Description: The BDI is a 21-item self-report inventory assessing depressive symptoms. Scores range from 0 to 63, with higher scores indicating greater severity of depression. Applied to all participants in both groups, with separate reporting for each assessment. Unit of Measure: Points on a scale (0-63)

Efficacy criteria

时间窗: Baseline (Week 1) and Post-intervention (Week 8)

Primary Outcome Measure 1 Title: Beck Anxiety Inventory (BAI) total score Time Frame: Baseline (Week 1) and Post-intervention (Week 8) Description: The BAI is a 21-item self-report questionnaire that measures the severity of anxiety symptoms. Total scores range from 0 to 63; higher scores indicate greater anxiety. Administered to all participants in both groups. Results will be reported separately for each time point. Unit of Measure: Points on a scale (0-63) Primary Outcome Measure 2 Title: Beck Depression Inventory (BDI) total score Time Frame: Baseline (Week 1) and Post-intervention (Week 8) Description: The BDI is a 21-item self-report inventory assessing depressive symptoms. Scores range from 0 to 63, with higher scores indicating greater severity of depression. Applied to all participants in both groups, with separate reporting for each assessment. Unit of Measure: Points on a scale (0-63)

次要结局

  • Efficacy criteria(Baseline (Week 1) and Post-intervention (Week 8))
  • Efficacy criteria(Baseline (Week 1) and Post-intervention (Week 8))

研究者

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

Luisa Pelucio Ribeiro Barbosa

Master - Principal Investigator

Universidade Federal do Rio de Janeiro

研究点 (1)

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