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Investigating Mindfulness and Music to Ease Radiation Side Effects in Prostate Cancer

Primary Purpose

Prostate Cancer

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Audio Program
Sponsored by
Northwestern University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Prostate Cancer focused on measuring prostate cancer, mindfulness, music

Eligibility Criteria

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

Inclusion Criteria:

  • Diagnosed with clinically localized prostate cancer
  • Will receive at least 7 weeks of daily radiation therapy
  • At least 18 years of age
  • Able to speak and understand English
  • Cognitively intact and free of serious psychiatric illness (as determined by referring physician)

Exclusion Criteria:

- Regular user of mindfulness meditation, which is defined as ≥ 3 times a week for the past 4 weeks

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Mindfulness Audio Program

    Music Audio Program

    Arm Description

    Mindfulness Audio Program is a daily audio-session, which teaches emotional self-regulation skills through the adoption of mindful awareness practices into one's life

    Music Audio Program is a daily audio session of peaceful and relaxing music

    Outcomes

    Primary Outcome Measures

    Implementation feasibility measured by enrollment rate
    This indicator of implementation feasibility for the program being delivered is defined by the overall enrollment rate being >/= 70% (e.g., total number of individuals enrolled/total number approached).
    Implementation feasibility measured by retention rate
    This indicator of implementation feasibility for the program delivered is defined by the retention rate being >/=70% (e.g., total number of individuals who remained in the trial until the end of requested participation/total number of individuals enrolled).
    Implementation feasibility measured by intervention adherence
    This indicator of implementation feasibility for the program delivered is defined by an adherence rate of >/=70% of all possible listening opportunities during the study intervention period.
    Program acceptability measured by a post-program survey at 4-weeks
    Program acceptability will be assessed using a brief, Likert-type survey assessing participant enjoyment, satisfaction, perceived benefit, and ease of use. Acceptability is defined as ≥70% of survey responses in affirmation of this.

    Secondary Outcome Measures

    Significant change in fatigue using the PROMIS Fatigue questionnaire
    Participants were administered the PROMIS Fatigue questionnaire. Significant change was indicated by a p<.05 on fatigue scores between baseline and follow up time points between study arms.
    Significant change in anxiety using the PROMIS Anxiety questionnaire
    Participants were administered the PROMIS Anxiety questionnaire. Significant change was indicated by a p<.05 on anxiety scores between baseline and follow up time points between study arms.
    Change in depression using the PROMIS Depression questionnaire
    Participants were administered the PROMIS Depression questionnaire. Significant change was indicated by a p<.05 on depression scores between baseline and follow up time points between study arms.
    Change in sleep using the PROMIS Sleep Disturbance questionnaire
    Participants were administered the PROMIS Sleep Disturbance questionnaire. Significant change was indicated by a p<.05 on sleep disturbance scores between baseline and follow up time points between study arms.
    Change in uncertainty intolerance using the Intolerance for Uncertainty Scale
    Participants were administered the Intolerance for Uncertainty questionnaire. Significant change was indicated by a p<.05 on uncertainty intolerance scores between baseline and follow up time points between study arms.
    Change in fear of recurrence using the MAX-PC Fear of Recurrence sub-scale
    Participants were administered the MAX-PC Fear of Recurrence questionnaire. Significant change was indicated by a p<.05 on fear of recurrence scores between baseline and follow up time points between study arms.
    Change in mindfulness using the Mindful Attention Awareness Scale
    Participants were administered the Mindful Attention Awareness Scale. Significant change was indicated by a p<.05 on mindfulness scores between baseline and follow up time points between study arms.

    Full Information

    First Posted
    December 12, 2018
    Last Updated
    May 4, 2023
    Sponsor
    Northwestern University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03852017
    Brief Title
    Investigating Mindfulness and Music to Ease Radiation Side Effects in Prostate Cancer
    Official Title
    IMMERSE PC: Investigating Mindfulness and Music to Ease Radiation Side Effects in Prostate Cancer
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2023
    Overall Recruitment Status
    Completed
    Study Start Date
    November 11, 2015 (Actual)
    Primary Completion Date
    January 8, 2018 (Actual)
    Study Completion Date
    January 8, 2018 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Northwestern University

    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
    In this study, the researchers will examine the implementation feasibility, acceptability, and initial effects of a brief eHealth mindfulness intervention, compared to brief relaxing music, to reduce self-reported symptoms of fatigue, anxiety, depression and sleep disturbance in a sample of localized prostate cancer patients during the receipt of radiation therapy.
    Detailed Description
    Eligible patients will be recruited from Northwestern Medicine's Department of Radiation Oncology and Northwestern Memorial Hospital. Participants will complete an online questionnaire prior to beginning the intervention. Following implementation pre-testing, the intervention will begin on Week 2 of radiation therapy and last 4 weeks. Upon arrival for their treatment visit, they will receive the audio program from the clinic staff. They will start the program prior to their treatment. Participants will be asked to listen to the audio-program during their radiation treatment visits, using a Bluetooth-enabled MP3 player with speaker instead of headphones or earbuds because they are not permitted during radiation therapy. The patient's ears need to be free to hear a possible communication from the radiation therapists if need be. Audio program recordings will run 3-12 minutes. Participants will turn off the program after their audio session has ended and return the audio program to the clinic staff after their treatment visit. Participants will complete an online question immediately after completing the intervention, and again 1 and 3 months later.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Prostate Cancer
    Keywords
    prostate cancer, mindfulness, music

    7. Study Design

    Primary Purpose
    Supportive Care
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Following implementation pre-testing, we will use a pilot randomized-controlled design to compare 2 groups: Group A: Mindfulness (n=25), a daily audio-session, which teaches emotional self-regulation skills through the adoption of mindful awareness practices into one's life; and Group B: Relaxing Music (n=25) - a daily audio session of peaceful and relaxing music. Participants will be assessed at baseline just prior to randomization to the two study arms (T1), followed by assessments at the end of the intervention period (T2), and 1 month (T3) and 3 months (T4) after the 4-week intervention period.
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    59 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Mindfulness Audio Program
    Arm Type
    Experimental
    Arm Description
    Mindfulness Audio Program is a daily audio-session, which teaches emotional self-regulation skills through the adoption of mindful awareness practices into one's life
    Arm Title
    Music Audio Program
    Arm Type
    Active Comparator
    Arm Description
    Music Audio Program is a daily audio session of peaceful and relaxing music
    Intervention Type
    Behavioral
    Intervention Name(s)
    Audio Program
    Primary Outcome Measure Information:
    Title
    Implementation feasibility measured by enrollment rate
    Description
    This indicator of implementation feasibility for the program being delivered is defined by the overall enrollment rate being >/= 70% (e.g., total number of individuals enrolled/total number approached).
    Time Frame
    Baseline
    Title
    Implementation feasibility measured by retention rate
    Description
    This indicator of implementation feasibility for the program delivered is defined by the retention rate being >/=70% (e.g., total number of individuals who remained in the trial until the end of requested participation/total number of individuals enrolled).
    Time Frame
    Throughout study completion, a total of four months.
    Title
    Implementation feasibility measured by intervention adherence
    Description
    This indicator of implementation feasibility for the program delivered is defined by an adherence rate of >/=70% of all possible listening opportunities during the study intervention period.
    Time Frame
    Throughout the study intervention period, a total of 4 weeks.
    Title
    Program acceptability measured by a post-program survey at 4-weeks
    Description
    Program acceptability will be assessed using a brief, Likert-type survey assessing participant enjoyment, satisfaction, perceived benefit, and ease of use. Acceptability is defined as ≥70% of survey responses in affirmation of this.
    Time Frame
    Week 4
    Secondary Outcome Measure Information:
    Title
    Significant change in fatigue using the PROMIS Fatigue questionnaire
    Description
    Participants were administered the PROMIS Fatigue questionnaire. Significant change was indicated by a p<.05 on fatigue scores between baseline and follow up time points between study arms.
    Time Frame
    baseline; Week 4; Month 1; Month 3
    Title
    Significant change in anxiety using the PROMIS Anxiety questionnaire
    Description
    Participants were administered the PROMIS Anxiety questionnaire. Significant change was indicated by a p<.05 on anxiety scores between baseline and follow up time points between study arms.
    Time Frame
    baseline; Week 4; Month 1; Month 3
    Title
    Change in depression using the PROMIS Depression questionnaire
    Description
    Participants were administered the PROMIS Depression questionnaire. Significant change was indicated by a p<.05 on depression scores between baseline and follow up time points between study arms.
    Time Frame
    baseline; Week 4; Month 1; Month 3
    Title
    Change in sleep using the PROMIS Sleep Disturbance questionnaire
    Description
    Participants were administered the PROMIS Sleep Disturbance questionnaire. Significant change was indicated by a p<.05 on sleep disturbance scores between baseline and follow up time points between study arms.
    Time Frame
    baseline; Week 4; Month 1; Month 3
    Title
    Change in uncertainty intolerance using the Intolerance for Uncertainty Scale
    Description
    Participants were administered the Intolerance for Uncertainty questionnaire. Significant change was indicated by a p<.05 on uncertainty intolerance scores between baseline and follow up time points between study arms.
    Time Frame
    baseline; Week 4; Month 1; Month 3
    Title
    Change in fear of recurrence using the MAX-PC Fear of Recurrence sub-scale
    Description
    Participants were administered the MAX-PC Fear of Recurrence questionnaire. Significant change was indicated by a p<.05 on fear of recurrence scores between baseline and follow up time points between study arms.
    Time Frame
    baseline; Week 4; Month 1; Month 3
    Title
    Change in mindfulness using the Mindful Attention Awareness Scale
    Description
    Participants were administered the Mindful Attention Awareness Scale. Significant change was indicated by a p<.05 on mindfulness scores between baseline and follow up time points between study arms.
    Time Frame
    baseline; Week 4; Month 1; Month 3

    10. Eligibility

    Sex
    Male
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Diagnosed with clinically localized prostate cancer Will receive at least 7 weeks of daily radiation therapy At least 18 years of age Able to speak and understand English Cognitively intact and free of serious psychiatric illness (as determined by referring physician) Exclusion Criteria: - Regular user of mindfulness meditation, which is defined as ≥ 3 times a week for the past 4 weeks
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    David E Victorson, PhD
    Organizational Affiliation
    Northwestern University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
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    Investigating Mindfulness and Music to Ease Radiation Side Effects in Prostate Cancer

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