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Efficacy of a Mindfulness-Based Intervention in Patients With Cardiovascular Implantable Electronic Device (MBI-CIED)

Primary Purpose

Mindfulness Training, Cardiac Resynchronization Therapy Devices, Resilience, Psychological

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
mindfulness-based intervention
CIED procedure routine care
Sponsored by
Chien Chih-Yin
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Mindfulness Training

Eligibility Criteria

18 Years - 100 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients receiving implanted cardiac devices for the first time (including cardiac defibrillator ICD and Pacemaker). Adults over 20 years old. Those who have clear consciousness and can communicate in Chinese and Taiwanese. Score of 8 or above on the Hospital Anxiety or Depression Scale. Barthel Index above 70 points. Exclusion Criteria: Diagnosed with dementia by a physician. Diagnosed with mental disorders, including cognitive disorders, organic psychosis and affective psychosis. Patients who have been diagnosed with cancer. Long-term bed ridden.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Other

    Arm Label

    mindfulness-based intervention and routine care

    The control group received the CIED procedure routine care

    Arm Description

    mindfulness-based intervention including: breathing awareness, body scanning, mindful yoga, mindful eating, and loving-kindness meditation. From the time when the patients signed up to be the first to receive the cardiac device surgery schedule, the experimental group that met the including criteria, in addition to following the routine care of the hospital, was involved in teaching the above mindfulness skills, and Osaka continued to follow the regular care.

    From the time when the patients signed up to be the first to receive the cardiac device surgery schedule, the control group that met the including criteria take routine care of the hospital.

    Outcomes

    Primary Outcome Measures

    Anxiety
    This study used the Hospital Anxiety and Depression Scale (HADS) to assess anxiety in patients. This scale provides anxiety (HADS-A) scores.
    Resilience
    This study uses the Connor-Davidson Resilience Scale (Connor-Davidson Resilience Scale), which was developed by Connor and Davidson (2003) in the United States who regarded resilience as a measurable stress response ability.
    Perceived Stress
    This study uses the Perceived Stress Scale, which was compiled by Cohen et al. (1983) and translated from the Chinese version of Chu and Gao (2005). , the degree of stress in life.
    Depression
    This study used the Hospital Anxiety and Depression Scale (HADS) to assess depression in patients. This scale provides anxiety (HADS-D) scores.

    Secondary Outcome Measures

    Demographic Information
    Collect age, gender, education level, marital status, occupation, smoking, drinking, disease history, other disease history, and exercise habits with self-made basic data sheets.
    body mass index
    weight and height will be combined to report BMI in kg/m^2
    Feelings and experiences by interview of home-based cardiac device patients receiving pre-procedure mindfulness intervention program
    Intentional sampling with phenomenological method. Conduct one-on-one interview recordings for the research subjects in the experimental group to collect the feelings and experiences of patients with implanted cardiac devices who received the mindfulness-based preoperative intervention program. It is expected to close the case until the data is saturated.

    Full Information

    First Posted
    June 29, 2023
    Last Updated
    August 31, 2023
    Sponsor
    Chien Chih-Yin
    Collaborators
    National Taipei University of Nursing and Health Sciences
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    1. Study Identification

    Unique Protocol Identification Number
    NCT06021236
    Brief Title
    Efficacy of a Mindfulness-Based Intervention in Patients With Cardiovascular Implantable Electronic Device
    Acronym
    MBI-CIED
    Official Title
    Efficacy of a Mindfulness-Based Intervention on Resilience, Perceived Stress, Anxiety, and Depression, in Patients With Cardiovascular Implantable Electronic Device: A Mixed-Methods Research
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    September 1, 2023 (Anticipated)
    Primary Completion Date
    December 30, 2024 (Anticipated)
    Study Completion Date
    December 30, 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor-Investigator
    Name of the Sponsor
    Chien Chih-Yin
    Collaborators
    National Taipei University of Nursing and Health Sciences

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    An implantable cardiac defibrillator (implantable cardioverter-defibrillator; ICD) can effectively improve heart rhythm problems and reduce sudden death, and is widely used in the treatment of high-risk patients with fatal arrhythmias or heart rhythm problems that cannot be controlled by drugs . In the whole case of arrhythmia, after receiving home-based cardiac fibrillator treatment, Patients often experience uncertainty, feel the changes in heart, feel the shock of being shocked by the electric shock, and worry about death, These psychological distress, which were characterized by anxiety and depression. for universal. About 25% of patients present with symptoms of anxiety at the time of hospitalization, and 50% suffer from depression which seriously affects quality of life. Therefore, the main purpose of this study to alleviate the occurrence of anxiety and depression, promote disease patients to regain life adaptation, develop accessible care strategies with midfulness-based intervention to help patients overcome psychological distress, reduce stress, anxiety and prevent depression.
    Detailed Description
    This study with randomized clinical trial design (randomized clinical trial) and qualitative research, which is a qualitative mixed-methods research. Patients were randomly assigned to the experimental group and the control group in a 1:1 manner. The experimental group received the mindfulness-based intervention designed and routine care , and the control group received general routine care. Both groups completed a total of four questionnaires at the pretest (T0), discharge (T1), the first month of discharge (T2), and the third month of discharge (T3), including anxiety, depression, resilience, stress perception scale and other basic data such as demographics and disease characteristics were collected in the pretest. This study held an expert meeting to extract the techniques of mindfulness measures suitable for this disease attribute and the elderly group, including: breathing awareness, body scanning, mindful yoga, mindful eating, and loving-kindness meditation. From the time when the patient signed up for the first cardiac device surgery schedule, the experimental group who met the including criteria followed the routine care of the hospital and was involved in teaching the above mindfulness skills, while the control group still followed the routine care.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Mindfulness Training, Cardiac Resynchronization Therapy Devices, Resilience, Psychological, Anxiety, Depression, Perceived Stress

    7. Study Design

    Primary Purpose
    Supportive Care
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    This study is a randomized clinical trial design (randomized clinical trial) with qualitative analysis, which is a mixed-methods research. Research objects were randomly assigned to the experimental and control groups in a 1:1 manner. The experimental group received the mindfulness-based intervention designed and routine care, and the control group received usual care. A total of four questionnaires were filled in the pretest (T0), the first month of discharge (T1), the 3rd month of discharge(T2), and the 6th month of discharge (T3), including anxiety, depression, mental toughness, and stress perception. Qualitative interviews were conducted at T2 and T3 to understand the improvement of psychological problems.
    Masking
    Participant
    Allocation
    Randomized
    Enrollment
    68 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    mindfulness-based intervention and routine care
    Arm Type
    Experimental
    Arm Description
    mindfulness-based intervention including: breathing awareness, body scanning, mindful yoga, mindful eating, and loving-kindness meditation. From the time when the patients signed up to be the first to receive the cardiac device surgery schedule, the experimental group that met the including criteria, in addition to following the routine care of the hospital, was involved in teaching the above mindfulness skills, and Osaka continued to follow the regular care.
    Arm Title
    The control group received the CIED procedure routine care
    Arm Type
    Other
    Arm Description
    From the time when the patients signed up to be the first to receive the cardiac device surgery schedule, the control group that met the including criteria take routine care of the hospital.
    Intervention Type
    Behavioral
    Intervention Name(s)
    mindfulness-based intervention
    Other Intervention Name(s)
    mindfulness-based intervention with CIED procedure routine care
    Intervention Description
    Diet meditation breath awareness body scan mindfulness yoga Compassionate blessing
    Intervention Type
    Other
    Intervention Name(s)
    CIED procedure routine care
    Intervention Description
    CIED procedure home care guidance
    Primary Outcome Measure Information:
    Title
    Anxiety
    Description
    This study used the Hospital Anxiety and Depression Scale (HADS) to assess anxiety in patients. This scale provides anxiety (HADS-A) scores.
    Time Frame
    From enrollment to the end of treatment at 6 months
    Title
    Resilience
    Description
    This study uses the Connor-Davidson Resilience Scale (Connor-Davidson Resilience Scale), which was developed by Connor and Davidson (2003) in the United States who regarded resilience as a measurable stress response ability.
    Time Frame
    From enrollment to the end of treatment at 6 months
    Title
    Perceived Stress
    Description
    This study uses the Perceived Stress Scale, which was compiled by Cohen et al. (1983) and translated from the Chinese version of Chu and Gao (2005). , the degree of stress in life.
    Time Frame
    From enrollment to the end of treatment at 6 months
    Title
    Depression
    Description
    This study used the Hospital Anxiety and Depression Scale (HADS) to assess depression in patients. This scale provides anxiety (HADS-D) scores.
    Time Frame
    From enrollment to the end of treatment at 6 months
    Secondary Outcome Measure Information:
    Title
    Demographic Information
    Description
    Collect age, gender, education level, marital status, occupation, smoking, drinking, disease history, other disease history, and exercise habits with self-made basic data sheets.
    Time Frame
    From enrollment to the end of treatment at 6 months
    Title
    body mass index
    Description
    weight and height will be combined to report BMI in kg/m^2
    Time Frame
    From enrollment to the end of treatment at 6 months
    Title
    Feelings and experiences by interview of home-based cardiac device patients receiving pre-procedure mindfulness intervention program
    Description
    Intentional sampling with phenomenological method. Conduct one-on-one interview recordings for the research subjects in the experimental group to collect the feelings and experiences of patients with implanted cardiac devices who received the mindfulness-based preoperative intervention program. It is expected to close the case until the data is saturated.
    Time Frame
    From enrollment to the end of treatment at 6 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    100 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients receiving implanted cardiac devices for the first time (including cardiac defibrillator ICD and Pacemaker). Adults over 20 years old. Those who have clear consciousness and can communicate in Chinese and Taiwanese. Score of 8 or above on the Hospital Anxiety or Depression Scale. Barthel Index above 70 points. Exclusion Criteria: Diagnosed with dementia by a physician. Diagnosed with mental disorders, including cognitive disorders, organic psychosis and affective psychosis. Patients who have been diagnosed with cancer. Long-term bed ridden.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Chih Yin Chien, PhD Candidates
    Phone
    +886-2-28584180
    Ext
    2234
    Email
    s157@mail.mkc.edu.tw
    First Name & Middle Initial & Last Name or Official Title & Degree
    TsaeJyy Wang, PhD
    Phone
    +886-2+28227101
    Ext
    3118
    Email
    tsaejyy@ntunhs.edu.tw
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Chih Yin Chien, PI
    Organizational Affiliation
    MKC/MMH
    Official's Role
    Study Chair

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    IPD Sharing Plan Description
    The research data belongs to the researcher and is expected to be destroyed after 2 years
    Citations:
    PubMed Identifier
    25519914
    Citation
    Freedenberg VA, Thomas SA, Friedmann E. A pilot study of a mindfulness based stress reduction program in adolescents with implantable cardioverter defibrillators or pacemakers. Pediatr Cardiol. 2015 Apr;36(4):786-95. doi: 10.1007/s00246-014-1081-5. Epub 2014 Dec 12.
    Results Reference
    result
    PubMed Identifier
    30204557
    Citation
    Hazlett-Stevens H, Singer J, Chong A. Mindfulness-Based Stress Reduction and Mindfulness-Based Cognitive Therapy with Older Adults: A Qualitative Review of Randomized Controlled Outcome Research. Clin Gerontol. 2019 Jul-Sep;42(4):347-358. doi: 10.1080/07317115.2018.1518282. Epub 2018 Sep 11.
    Results Reference
    result
    PubMed Identifier
    30295057
    Citation
    Hopgood DA, Czosek RJ, Bakas T, Garritano N, Gillespie GL. The Capture Gap: Implantable Cardioverter-Defibrillator Quality of Life. Clin Nurs Res. 2020 Feb;29(2):97-107. doi: 10.1177/1054773818803741. Epub 2018 Oct 7.
    Results Reference
    result
    PubMed Identifier
    30656813
    Citation
    Li SYH, Bressington D. The effects of mindfulness-based stress reduction on depression, anxiety, and stress in older adults: A systematic review and meta-analysis. Int J Ment Health Nurs. 2019 Jun;28(3):635-656. doi: 10.1111/inm.12568. Epub 2019 Jan 17.
    Results Reference
    result
    PubMed Identifier
    34072605
    Citation
    Marino F, Failla C, Carrozza C, Ciminata M, Chila P, Minutoli R, Genovese S, Puglisi A, Arnao AA, Tartarisco G, Corpina F, Gangemi S, Ruta L, Cerasa A, Vagni D, Pioggia G. Mindfulness-Based Interventions for Physical and Psychological Wellbeing in Cardiovascular Diseases: A Systematic Review and Meta-Analysis. Brain Sci. 2021 May 29;11(6):727. doi: 10.3390/brainsci11060727.
    Results Reference
    result
    PubMed Identifier
    33372277
    Citation
    Rafsanjani MHAP, Masoudi S, Radmanesh M, Bostani Z. Comparison of depression and anxiety among pacemaker and implantable cardioverter-defibrillator recipients: A cross-sectional study. Pacing Clin Electrophysiol. 2021 Feb;44(2):235-239. doi: 10.1111/pace.14152. Epub 2021 Jan 12.
    Results Reference
    result
    PubMed Identifier
    30957867
    Citation
    Schulz SM, Ritter O, Zniva R, Nordbeck P, Wacker C, Jack M, Groschup G, Deneke T, Puppe F, Ertl G, Angermann C, Stork S, Pauli P. Efficacy of a web-based intervention for improving psychosocial well-being in patients with implantable cardioverter-defibrillators: the randomized controlled ICD-FORUM trial. Eur Heart J. 2020 Mar 14;41(11):1203-1211. doi: 10.1093/eurheartj/ehz134.
    Results Reference
    result

    Learn more about this trial

    Efficacy of a Mindfulness-Based Intervention in Patients With Cardiovascular Implantable Electronic Device

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