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Completed

NCT Number: NCT05967247

MBSR on Physiological and Psychological Factors in Patients With HF

Objective

The purpose of this study is to explore the relationship between mindfulness, resilience, depression and quality of life in patients with heart failure, and the effect of mindfulness-based stress reduction intervention with mobile phone application on subjects with depressive symptoms. Therefore, the research objectives are as follows:

1. To explore the relationship between mindfulness, resilience, depression, and quality of life in patients with heart failure, and to explore the mediating role of positive emotions (mindfulness, resilience). 2. Using a mobile phone app to conduct mindfulness-based stress reduction interventions, to explore the effects of physiological and psychological factors in heart failure patients with depressive symptoms.

Methods This study will be conducted in two parts. The first part will be a cross-sectional study. It is planned to be conducted in the cardiology ward or outpatient clinic of a university-affiliated hospital in northern Taiwan between September and December 2023 after the approval of the Human Experiment Ethics Committee. Contact the patients who meet the research conditions, adopt the intentional sampling method, and plan to accept 180 research objects for the questionnaire survey, the collection tools are the basic information of the research objects, mindfulness, resilience, depression, quality of life scale; in the first part, the patients' Health Questionnaire (patient health questionnaire-9, PHQ-9) was used to screen for depressive symptoms, and when the total score ≧ 5 points, they were invited to participate in the second part of the study. The second part plans to include 68 subjects in the study, adopting a single-blind random allocation waiting list design, using the app designed by the researcher to implement the mindfulness-based stress reduction intervention program, which is planned to be carried out for 8 weeks, and since the beginning of the study, the 8th week (After the intervention in the experimental group), and the 16th week (after the intervention in the control group), a total of three research data collections were carried out.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

National Taiwan University Hospital

Taipei, 100225, Taiwan

About this study

Expected research results The expected results of the first part of the research are that the research subjects with higher mindfulness have less depression, higher resilience, and better quality of life, and the mindfulness of the research subjects can play a mediating role between depression and quality of life; the second part expects the research subjects After receiving the intervention of mindfulness-based stress reduction on the mobile phone application, it can increase their mindfulness, resilience and quality of life, reduce depression, blood pressure, and improve heart rate variability.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

  • Inclusion Criteria:
  • (1) The diagnosis of heart failure is confirmed by a clinician, and the definition of the diagnosis is based on the international statistical classification of diseases and related health problems 10th revision (ICD-10), including I50 Heart failure ( heart failure) related diagnostic codes.
  • (2) Legally recognized as an adult ≧ 18 years old.
  • (3) The second part of the experimental research, in addition to the above inclusion conditions, also needs to have a patient health questionnaire ≥ 5 points, which means mild or above (including) depression (Kroenke et al., 2001; Yeung et al., 2008) can be included in the study.
  • Exclusion Criteria:
  • (1) Diagnosed by a physician as having depression or taking antidepressant drugs regularly, such as selective serotonin reuptake inhibitor (SSRI), serotonin and norepinephrine reuptake inhibitor (serotonin-norepinephrine reuptake inhibitors (SNRI), tricyclic antidepressants (TCA), monoamine oxidase inhibitors (monoamine oxidase inhibitor, MAOI), tetracyclic antidepressants (TeCA), norepinephrine And specific serotonergic antidepressants (Noradrenergic and specific serotonergic antidepressants, NaSSA).
  • (2) New York heart association functional classification (NYHA Fc) IV, which means that it is uncomfortable to perform any physical activity, even when lying in bed or moving, you may feel symptoms such as dyspnea or palpitations.
  • (3) Those who still need to use oxygen or breathing aids throughout the day.
  • (4) Those who are still equipped with ventricular assist devices and rely on life-support devices.
  • (5) Activities of daily living (ADL) < 60 points, unable to take care of themselves in daily life.
  • (6) For those with abnormal cognitive function, the mini-mental state examination (MMSE) < 24 points.
  • (7) Those who have undergone heart transplantation have lost innervation because there is no connection between the autonomic nerve and the heart (McCraty & Shaffer, 2015).
  • (8) In the second part of the interventional experimental research, in addition to the above exclusion conditions, in order to avoid interference with the research, it is also necessary to exclude:
  • A. Those who cannot read traditional Chinese or communicate in Mandarin or Taiwanese, because health education-related materials, videos and applications are all in traditional Chinese.
  • B. Those who cannot use Android devices at home with smartphones or tablets need to operate the application at home due to intervention measures.
  • C. Those who have regularly taken measures related to mindfulness, meditation, and sitting meditation in the past year are not included in order to avoid interfering with the research results.

Treatment and study plan

The experimental group used App for MBSR intervention

Other

The experimental group used App for MBSR intervention The main app of this experiment is "Mindfulness in Life (Taiwan)" (this system is only applicable to Android devices). The content is divided into two parts. The course is compressed and simplified, mainly focusing on mindfulness learning and practicing audio-visuals. There are eight-week themed audio-visuals and mindful caring words guided by mindfulness-based stress reduction, mindfulness-stretching guidance, and the function of recording the reading time of the research subjects. App platform for researchers to communicate.

Other names: Control group serves as a waiting list with priority given to placebo Placebo for the "Heart Care Life" app.

the "Heart Care Life" app

Other

Control group serves as a waiting list with priority given to placebo Placebo for the "Heart Care Life" app.

App

Other

APP

Primary outcomes

  1. quality of life (SF-12v2)

    Time frame: T0, T1 = 8 weeks, T2 = 16 weeks.

    short-form health survey (SF-12v2), Cronbach's α = 0.76~0.85.

Secondary outcomes

  1. depression

    Time frame: T0, T1 = 8 weeks, T2 = 16 weeks.

    patient health questionnaire (PHQ-9), Cronbach's α = 0.84

  2. mindfulness

    Time frame: T0, T1 = 8 weeks, T2 = 16 weeks.

    five facet mindfulness questionnaire-short form (FFMQ-SF), Cronbach's α= 0.69~0.85.

  3. Resilience

    Time frame: T0, T1 = 8 weeks, T2 = 16 weeks.

    Connor-Davidson resilience scale (CD-RISC-10), Cronbach's α = 0.94

Other outcomes

  1. medication adherence

    Time frame: T0, T1 = 8 weeks, T2 = 16 weeks.

    Medication Adherence Self-Reported by Patient

  2. Heart rate variability (HRV)

    Time frame: T0, T1 = 8 weeks, T2 = 16 weeks.

    Measured with a non-plunging wrist-worn instrument

  3. heart rate (pulse)

    Time frame: T0, T1 = 8 weeks, T2 = 16 weeks.

    Measured according to the blood pressure measuring instrument regularly calibrated by the hospital

  4. blood pressure (BP)

    Time frame: T0, T1 = 8 weeks, T2 = 16 weeks.

    Measured according to the blood pressure measuring instrument regularly calibrated by the hospital

Sponsors and collaborators

Lead sponsor

National Taiwan University Hospital

Other

Registry information

Official study title

The Effect of App-Based Mindfulness-Based Stress on Physiological and Psychological Factors in Patients With Heart Failure: A Randomized Controlled Trial

Acronym: MBSR-PP-HF

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Aug 1, 2023
Registry last updated
Dec 27, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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