Combined Cognitive Bias Modification for Perfectionism and Intolerance to Uncertainty: A Randomized Controlled Trial
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 54
- 试验地点
- 2
- 主要终点
- Change in Brief Symptom Measure
研究概览
简要总结
This study will examine the impact of cognitive bias modification (CBM) on perfectionism and intolerance to uncertainty. Undergraduate students will be recruited and randomly assigned to either experimental or placebo-control groups. Each group will attend four sessions of CBM over four weeks.
详细描述
Background. Cognitive bias modification (CBM) is an intervention aiming to systematically change the biases in cognitive processing using experimental paradigms. CBM was found effective with a variety of disorders and transdiagnostic variables. Although there are few studies focusing on transdiagnostic variables like perfectionism and intolerance to uncertainty, further research needs to be done for the generalizability of these results. It was aimed in this study to test the effectiveness of CBM for perfectionism and intolerance to uncertainty with a sample of undergraduate students in Turkey.
Sample size was determined using G*power for a medium to large effect size based on previous studies and it was planned to include 28 undergraduate students who have a score of >70.5 in the Brief Symptom Measure in the study. Participants will get either 3-course credits or a 100 TL bookstore gift card for their full participation. After getting informed consent from participants, they will be randomized to either active or control condition. Participants will be blind to their intervention condition. Following randomization, baseline measurements will be collected. After the baseline measures were collected, links for interventions will be e-mailed to the participants according to their assigned group. Participants will get an email including the link for the study every week. Interpretation bias scores of participants for perfectionism and intolerance to uncertainty will be collected before the first intervention session and after the last intervention session. These sessions will last approximately 25 min. Participants will attend the session without an assessment in the second and third week and these sessions will last approximately 15 min. After four sessions, post-tests will be sent to the participants. Questionnaires will also be collected one month after the intervention was done.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Double (Participant, Care Provider)
盲法说明
Participants will be blinded to their assigned condition. They will have ID numbers created by random.org which will allow the care provider to be blinded to the assigned conditions of participants.
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
- •Older than 18 years old
- •Have a score of >70.5 in Brief Symptom Measure
- •Being an undergraduate student
- •Fluent in Turkish
- •Access to the internet by computer
排除标准
- •Having any psychiatric disorder
- •Receiving a psychiatric/psychological treatment
结局指标
主要结局
Change in Brief Symptom Measure
时间窗: Weeks 0, 4, 8
Psychiatric symptomatology will be assessed with Brief Symptom Measure consists of 25 items scored 1-7. Greater score means greater severity.
次要结局
- Change in Interpretation bias for perfectionism(Weeks 0, 4)
- Change in Intolerance of Uncertainty Scale(Weeks 0, 4, 8)
- Change in Frost Multidimensional Perfectionism Scale(Weeks 0, 4, 8)
- Change in Cognitive-Behavioral Avoidance Scale(Weeks 0, 4, 8)
- Change in Interpretation bias for intolerance to uncertainty(Weeks 0, 4)
研究者
Kübra Tör
MA
Istanbul Sabahattin Zaim University
