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临床试验/NCT06817473
NCT06817473已完成不适用

Evaluation of the Feasibility and Efficacy of Computerized Anxiety Treatment in a Group Setting - RCT

Florida State University1 个研究点 分布在 1 个国家目标入组 73 人开始时间: 2024年2月21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
73
试验地点
1
主要终点
Treatment Engagement Questionnaire

研究概览

简要总结

  • Statement of the Research Study. Participants are being invited to volunteer to take part in our research study. It is up to participants whether to choose to take part or not. There will be no penalty or loss of benefits to choosing not to take part or decide later not to take part.
  • Purpose. The reason that the researchers are doing this research is to evaluate the effectiveness and feasibility of administering a computerized anxiety intervention in a setting of five or more individuals. This intervention has already been tested and shown promise with individuals, and researchers want to see if it will function in a group setting as well.
  • Duration. Researchers think that taking part in our study will last approximately two hours, with an additional follow-up survey one month later to be completed at home via computer or smartphone.
  • Research Activities. Participants will first be asked to complete several questionnaires dealing with your thoughts and feelings. Once these questionnaires are completed, participants will be assigned to one of two groups, with each group viewing one of two computerized presentations and completing some group exercises afterward. Once participants have completed the designated intervention, participants will then be asked to fill out surveys once again, which will complete the study appointment. One month following the appointment, participants will be sent surveys once again and will be asked to complete them at home.

Risks: The risks or discomforts to participants while taking part in this research include temporary distress or anxiety pr potentially feeling mild discomfort answering questions about your thoughts and feelings.

Benefits: As a result of taking part in this research, participants may experience improvements in mental health.

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 (Participant)

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

  • •adults aged 18+ and ability to use a computer or smartphone.

排除标准

  • •inability to engage in any interoceptive exercises.

研究组 & 干预措施

CAST

Experimental

Computerized anxiety sensitivity treatment (CAST), which has been used by researchers already in many RCTs. This involves 30 minutes of psychoeducational video material delivered via computer presentation followed by 30 minutes of repeated interoceptive exposure practice exercises such as 60 seconds of breathing through a coffee straw, shaking head from side to side, and looking into a mirror.

干预措施: CAST (Behavioral)

HET

Placebo Comparator

Developed as a 30-minute online intervention that provides education about physical health habits that can impact mental health, such as diet, exercise, and sleep. This intervention has been used in prior clinical trials to control for effects of general education, general coping techniques, and use of technology. Participants in past clinical trials have reported that HET is engaging and beneficial.

干预措施: HET (Behavioral)

结局指标

主要结局

Treatment Engagement Questionnaire

时间窗: Month 1 Follow Up

Participants were given two items assessing how frequently they: 1) thought about CAST content in the past month; 2) engaged in interoceptive exposure practice.

PROMIS Depression Scale 8b

时间窗: Baseline through Month 1 Follow Up

8 item self-report measure indexing depressive symptoms (Polkonis et al., 2014). Scores range from 8-40 with higher scores reflecting worse depression symptoms.

Treatment Acceptability Questionnaire

时间窗: Baseline through Month 1 follow up

7-item self-report measure used in prior studies (Short et al., 2017). Scores range from 0-21 with higher scores indicating more favorable acceptability ratings.

Anxiety Sensitivity Index-3

时间窗: Baseline through Month 1 follow up

18 item self-report measure indexing anxiety sensitivity (Taylor et al., 2007). Scores range from 0-72 with higher scores indicating more severe anxiety sensitivity

PROMIS Anxiety Scale 8a

时间窗: Baseline through Month 1 Follow Up

8-item self-report measure indexing overall anxiety (Pilkonis et al., 2011). Scores range from 8 to 40 with higher scores reflecting worse anxiety symptoms.

次要结局

  • Client Satisfaction Questionnaire(Baseline through Month 1 Follow Up)
  • Intolerance of Uncertainty-12(Baseline through Month 1 follow up)
  • Difficulties in Emotion Regulation Scale(Baseline through Month 1 follow up)

研究者

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

Norman Schmidt

Distinguished Research Professor

Florida State University

研究点 (1)

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