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Cardiac Coherence Combined With Personal Physical Activity in Patients With Cancer (APACCHE)

Primary Purpose

Physical Activity, Cancer, Hematologic Diseases

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Cardiac Coherence
Adapted Physical Activity
Sponsored by
Centre Hospitalier Universitaire de la Réunion
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Physical Activity

Eligibility Criteria

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

Inclusion Criteria:

  • All patients, previously treated and in remission for an Hematologic malignancy, in whom APA is indicated.
  • Adult patients aged 18-65 yo
  • Followed at South University Hospital of La Réunion Island
  • Previously treated for Hematologic Malignancy, and in Remission (complete or partial)
  • 6 months or less since last treatment
  • Hemoglobin steady ≥ 90g/L
  • In whom APA is prescribed
  • Ability to give oral informed consent
  • French understanding

Exclusion Criteria:

  • With contraindication for APA
  • Under anti-arhythmic or beta-blocker drugs
  • Cardiac insufficiency (Left ventriculi Ejection Fraction less than 40%)
  • Participation in another trial

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Cardiac Coherence

    Adapted Physical Activity

    Arm Description

    Patients participate to Adapted physical activity sessions and to cardiac coherence sessions

    Patients only participate to Adapted physical activity sessions

    Outcomes

    Primary Outcome Measures

    Health-related quality of life
    Health-related quality is assessed by the Quality of Life Questionnaire dedicated to cancer patients and including 30 items (QLQ-C30) developed by the European Organization for Research and Treatment of Cancer (EORTC). This questionnaire is a multimodal construct, typically including physical, emotional and psychological health issues; evaluated with the QLQ-C30 survey of the European Organization for Research and Treatment of Cancer. QLQ-C30 items are coded with the same response categories as items 6 to 28, namely "Not at all", "A little", "Quite a bit" and "Very much." Score ranges from 0 to 100, with higher score indicating higher levels of quality of life.

    Secondary Outcome Measures

    Fatigue improvement
    Fatigue improvement is assessed by multidimensional fatigue inventory (MFI-20 survey). MFI-20 consists of five subscales used to express: general fatigue, physical, reduced activities, reduced motivation, mental fatigue. Each scale contains four items for which the person had to indicate the extent the items describe their situations in the recent few days on a 5-point Likert scale, ranging from "yes, that is true" to "no, that is not true" Scores on each subscale range from 4 to 20, with higher scores indicating higher levels of fatigue.
    Anxiety and depression improvement with Hospital Anxiety and Depression Scale (HADS) survey
    Anxiety and depression improvement is assessed by HADS survey. The HADS is a fourteen item scale that generates ordinal data. Seven of the items relate to anxiety and seven relate to depression. Each item on the questionnaire is scored from 0-3: a person can score between 0 and 21 for either anxiety or depression. Higher scores indicate higher levels of depression or anxiety
    Cardiac coherence improvement
    Increased percentage of cardiac coherence is measured with SYMBIOLINE software

    Full Information

    First Posted
    November 23, 2017
    Last Updated
    December 18, 2017
    Sponsor
    Centre Hospitalier Universitaire de la Réunion
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03356171
    Brief Title
    Cardiac Coherence Combined With Personal Physical Activity in Patients With Cancer
    Acronym
    APACCHE
    Official Title
    Combination of Cardiac Coherence to Physical Activity
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2017
    Overall Recruitment Status
    Unknown status
    Study Start Date
    January 2018 (Anticipated)
    Primary Completion Date
    March 2019 (Anticipated)
    Study Completion Date
    June 2019 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Centre Hospitalier Universitaire de la Réunion

    4. Oversight

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

    5. Study Description

    Brief Summary
    APACCHE (Adapted Physical Activity and Cardiac Coherence in HEmatologic patients) study investigates effects of heart rate variability biofeedback training, combined with classical adapted physical activity, on health-related quality of life in patients previously treated for hematologic malignancies. It is a prospective, randomized clinical trial from University Hospital of Reunion Island. The main objective is evaluated with QLQ-C30 survey score differences.
    Detailed Description
    Hematologic malignancies are aggressive cancers with significant long-term effects on physical and psychological health, due to the disease itself or aggressive treatments. Physical activity, with specific treatments, improves physical and psychological health in solid tumors patients. However, in hematologic malignancies, there is unsatisfactory quality of evidence that physical activity alone improves the various dimensions of quality of life. Recent studies on heart-brain connections suggest that a high level of coherence in the heart rate variability may induce psychophysiological positive effects. Cardiac coherence is reached when the heart rhythm pattern becomes sine-wave-like at a frequency around 0.1 Hz. This status can be increased by the mean of deep and slow breathing control and/or positive emotions. By using a heart rate variability biofeedback training, previous studies have shown effects on physiological variables such as reduction of blood pressure or increase of vagal heart rate control, and also on psychological variables such as reduction of stress, anxiety, and depression. The APACCHE protocol investigate if cardiac coherence biofeedback training, associated with an adapted physical activity program, can improve health related quality of life in adult hematologic patients. 70 patients are randomly assigned to receive either ten sessions of cardiac coherence biofeedback (CC-BF) and the adapted physical activity program (APA) or just APA. Both interventions are conducted simultaneously over 12 weeks, with 10 sessions of CC-BF (45mn) weekly and 24 sessions of APA (1h30) bi-weekly. Data are collected at enrollment(T1), at 6 weeks (T2), at intervention ending at 12 weeks (T3) and after a 24 weeks follow-up (T4).

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Physical Activity, Cancer, Hematologic Diseases

    7. Study Design

    Primary Purpose
    Supportive Care
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Outcomes Assessor
    Allocation
    Randomized
    Enrollment
    70 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Cardiac Coherence
    Arm Type
    Experimental
    Arm Description
    Patients participate to Adapted physical activity sessions and to cardiac coherence sessions
    Arm Title
    Adapted Physical Activity
    Arm Type
    Active Comparator
    Arm Description
    Patients only participate to Adapted physical activity sessions
    Intervention Type
    Procedure
    Intervention Name(s)
    Cardiac Coherence
    Intervention Description
    10 sessions of HRV-BF (45mn) weekly over 12 weeks. HRV-BF is a cognitive behavioural therapy consisting on stress management training based on breathing. We use the SYMBIOLINE PC software to record the heart rate variability biofeedback, with an infrared plethysmograph sensor. The sensor is put on the finger, and the patient's HRV pattern is displayed in real time. 24 APA sessions (1.5h) bi-weekly over 12 weeks. Each session includes aerobic exercises (walk, step) and resistant exercises (muscular reinforcement). This program is built on previous cancer studies to make it effective.
    Intervention Type
    Procedure
    Intervention Name(s)
    Adapted Physical Activity
    Intervention Description
    - 24 APA sessions (1.5h) bi-weekly over 12 weeks. Each session includes aerobic exercises (walk, step) and resistant exercises (muscular reinforcement). This program is built on previous cancer studies to make it effective.
    Primary Outcome Measure Information:
    Title
    Health-related quality of life
    Description
    Health-related quality is assessed by the Quality of Life Questionnaire dedicated to cancer patients and including 30 items (QLQ-C30) developed by the European Organization for Research and Treatment of Cancer (EORTC). This questionnaire is a multimodal construct, typically including physical, emotional and psychological health issues; evaluated with the QLQ-C30 survey of the European Organization for Research and Treatment of Cancer. QLQ-C30 items are coded with the same response categories as items 6 to 28, namely "Not at all", "A little", "Quite a bit" and "Very much." Score ranges from 0 to 100, with higher score indicating higher levels of quality of life.
    Time Frame
    on week 12
    Secondary Outcome Measure Information:
    Title
    Fatigue improvement
    Description
    Fatigue improvement is assessed by multidimensional fatigue inventory (MFI-20 survey). MFI-20 consists of five subscales used to express: general fatigue, physical, reduced activities, reduced motivation, mental fatigue. Each scale contains four items for which the person had to indicate the extent the items describe their situations in the recent few days on a 5-point Likert scale, ranging from "yes, that is true" to "no, that is not true" Scores on each subscale range from 4 to 20, with higher scores indicating higher levels of fatigue.
    Time Frame
    through study completion: initially (T1), at 6 weeks (T2), 12 weeks (T3) and after at 24 weeks (T4) follow-up
    Title
    Anxiety and depression improvement with Hospital Anxiety and Depression Scale (HADS) survey
    Description
    Anxiety and depression improvement is assessed by HADS survey. The HADS is a fourteen item scale that generates ordinal data. Seven of the items relate to anxiety and seven relate to depression. Each item on the questionnaire is scored from 0-3: a person can score between 0 and 21 for either anxiety or depression. Higher scores indicate higher levels of depression or anxiety
    Time Frame
    through study completion: initially (T1), at 6 weeks (T2), 12 weeks (T3) and after at 24 weeks (T4) follow-up
    Title
    Cardiac coherence improvement
    Description
    Increased percentage of cardiac coherence is measured with SYMBIOLINE software
    Time Frame
    through study completion: initially (T1), at 6 weeks (T2), 12 weeks (T3) and after at 24 weeks (T4) follow-up

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: All patients, previously treated and in remission for an Hematologic malignancy, in whom APA is indicated. Adult patients aged 18-65 yo Followed at South University Hospital of La Réunion Island Previously treated for Hematologic Malignancy, and in Remission (complete or partial) 6 months or less since last treatment Hemoglobin steady ≥ 90g/L In whom APA is prescribed Ability to give oral informed consent French understanding Exclusion Criteria: With contraindication for APA Under anti-arhythmic or beta-blocker drugs Cardiac insufficiency (Left ventriculi Ejection Fraction less than 40%) Participation in another trial
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Christine JUHEL, PHD
    Phone
    +262262359949
    Email
    christine.juhel@chu-reunion.fr
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Quentin CABRERA, MD
    Organizational Affiliation
    Centre Hpospitalier Universitaire de La REUNION
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    32190333
    Citation
    Fournie C, Bouscaren N, Dalleau G, Lenclume V, Mohr C, Zunic P, Cabrera Q, Verkindt C. Adapted physical activity and cardiac coherence in hematologic patients (APACCHE): study protocol for a randomized controlled trial. BMC Sports Sci Med Rehabil. 2020 Mar 14;12:18. doi: 10.1186/s13102-020-00170-3. eCollection 2020.
    Results Reference
    derived

    Learn more about this trial

    Cardiac Coherence Combined With Personal Physical Activity in Patients With Cancer

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