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临床试验/NCT04983680
NCT04983680已完成1 期

Remote-delivered Mindfulness-Based Cognitive Therapy to Target Fear of Recurrence Among SCAD Survivors

Massachusetts General Hospital2 个研究点 分布在 1 个国家目标入组 19 人开始时间: 2021年11月4日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
19
试验地点
2
主要终点
Feasibility of Enrollment: Percent of Participants Enrolled

研究概览

简要总结

Spontaneous coronary artery dissection (SCAD) is an important cause of cardiac events, primarily affecting young healthy women with no cardiovascular risk factors. The 10-year recurrence rate is 30%, but SCAD recurrence cannot be predicted. Approximately half of SCAD survivors struggle with significant anxiety and fear of recurrence (FOR), which contributes to poor sleep and physical inactivity and, thereby, increased risk of recurrence. Mindfulness-Based Cognitive Therapy (MBCT) is an 8-week group intervention with evidence to improve FOR and health behaviors (sleep, physical activity), through psychological mechanisms that directly target key FOR processes (interoceptive bias, intolerance of uncertainty). I adapted MBCT to target FOR, sleep, and physical activity in cardiac event survivors via group videoconferencing delivery (UpBeat-MBCT), however this intervention has not yet been targeted to SCAD survivors. I propose an open pilot trial to test the feasibility, acceptability, and changes in psychological and behavioral health variables in SCAD survivors participating in UpBeat-MBCT (N=16). Participants will be recruited from the MGH SCAD Program and asked to complete self-report surveys and actigraphy before and after the intervention. The primary outcomes are feasibility and acceptability of the intervention and research procedures. Exploratory outcomes are changes in psychological and behavioral variables and their inter-correlations. This project would be the first and only behavioral intervention for SCAD survivors and would provide preliminary data for an NIH Stage II efficacy trial to develop an accessible and efficacious intervention for a vulnerable group of SCAD survivors, with generalizability to survivors of other cardiac events.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
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

入选标准

  • Age >18 years
  • Cardiologist-confirmed diagnosis of SCAD in the past 1-12 months
  • English-speaking and reading
  • Internet access (via computer or mobile device).

排除标准

  • Terminal illness with life expectancy <1 year
  • Severe mental illness requiring urgent psychiatric intervention (e.g., active suicidal ideation) or past-year psychiatric hospitalization)
  • Significant cognitive impairment preventing informed consent determined by study staff or medical record review (e.g., medical history of cognitive impairment)
  • Deemed unable to complete research procedures (e.g., group sessions or surveys) per clinical judgment of study staff
  • Unavailable for intervention sessions (e.g., schedule conflicts)

结局指标

主要结局

Feasibility of Enrollment: Percent of Participants Enrolled

时间窗: 7 months

Feasibility will be assessed by \>70% of eligible patients enroll

Feasibility of Videoconferencing Delivery: Percent of Sessions With Videoconferencing Problems

时间窗: 7 months

Feasibility of videoconferencing delivery will be assessed by \<20% of sessions missed due to videoconference problems

Intervention Acceptability: Plans to Use the Skills in the Future

时间窗: 7 months

Intervention acceptability will be assessed by \>70% plan to use the intervention skills in the future

Feasibility of MBCT Intervention: Participant Attendance Rates

时间窗: 7 months

Feasibility of UpBeat-MBCT intervention will be assessed by \>70% of participants attending \>6/8 sessions

Intervention Acceptability: Would Recommend the Program to Others

时间窗: 7 months

Intervention acceptability will be assessed by \>70% would recommend the program to others

Acceptability of Daily Diary Surveys: Level of Survey Interference

时间窗: 7 months

Acceptability of daily diaries will be assessed by level of survey interference in daily life (1=not at all, 10=extremely, M\<2.0)

Acceptability of Actigraphy

时间窗: 7 months

Acceptability of actigraphy will be assessed by ratings of ease of actigraphy completion (1=not at all, 10 =extremely, M\>7.0)

Feasibility of Actigraphy Use: Percent of Participants Who Adhere to Actigraphy Procedures at Post-intervention

时间窗: 7 months

Feasibility of actigraphy use will be assessed by \>70% of participants completing actigraphy for 7 consecutive days at post-intervention

Feasibility of Retention: Percent of Enrolled Participants Retained at Post-intervention

时间窗: 7 months

Feasibility of retention will be assessed by \> 70% of participants completing the post-intervention survey

Feasibility of Daily Diaries: Percent of Participants Who Complete the Daily Diaries at Pre-intervention

时间窗: 7 months

Feasibility of daily diary completion will be assessed by \>70% of participants completing daily diaries for 7 consecutive days at pre-intervention

Feasibility of Daily Diaries: Percent of Participants Who Complete the Daily Diaries at Post-intervention

时间窗: 7 months

Feasibility of daily diary completion will be assessed by \>70% of participants completing daily diaries for 7 consecutive days at post-intervention

Feasibility of Actigraphy Use: Percent of Participants Who Adhere to Actigraphy Procedures at Pre-intervention

时间窗: 7 months

Feasibility of actigraphy use will be assessed by \>70% of participants completing actigraphy for 7 consecutive days at pre-intervention

Intervention Acceptability: Home Practice Completion

时间窗: 7 months

Acceptability of the UpBeat-MBCT intervention will be assessed by \>70% of participants completing home practice \>3days/week

Acceptability of Daily Diary Surveys: Ease of Completion

时间窗: 7 months

Acceptability of daily diaries will be assessed by ease of daily diary completion (1=not at all, 10=extremely). Mean acceptability rating \> 7.0 indicates acceptability

次要结局

  • Fear of Recurrence(7 months)
  • Self-reported Sleep Outcomes(3 months)
  • Distress Tolerance(7 months)
  • Cardiac Anxiety(7 months)
  • Non-judgmental Body Awareness(7 Months)
  • Cognitive De-centering(7 months)
  • Attention Regulation(7 months)
  • Interoceptive Bias(7 months)
  • Intolerance of Uncertainty(7 months)
  • Self-reported Physical Activity(3 months)

研究者

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

Christina Luberto

Assistant Professor of Psychology

Massachusetts General Hospital

研究点 (2)

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