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The Effect of Prayer on Dyspnea Severity, Anxiety and Spiritual Well-Being in Individuals With COPD (COPD)

Primary Purpose

COPD

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
A prayer concert will be held for the participants.
Sponsored by
Cumhuriyet University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for COPD focused on measuring DYSPNEA, SPIRITUAL GOODNESS, ANXIETY

Eligibility Criteria

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

Inclusion Criteria: 90 individuals (45 experiments, 45 controls) who can be contacted, who have agreed to participate in the study who are literate, can speak Turkish who have not participated in a similar application of this study before who have agreed to participate in the study after being informed about the research are 18 years old and over, with a COPD diagnosis will be taken Exclusion Criteria: Individuals with mental and hearing problems, who have lost a family member and someone close to them in the last year who are using tranquilizers/antidepressants who have experienced a traumatic situation such as divorce will be excluded from the sample.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    Experimental Group

    Control Group

    Arm Description

    Participants in this group will be given a prayer concert for a month. At the end of one month, the severity of dyspnea, anxiety and spiritual well-being levels experienced by the participants will be re-checked.

    There will be no prayer audience for participants in this group.

    Outcomes

    Primary Outcome Measures

    dyspnea 12 scale
    as a result of 1-month prayer listening, the severity of dyspnea of the participants in the experimental group decreased. A minimum of 0 and a maximum of 36 points are taken from the scale. The increase in scores indicates that the frequency of dyspnea of patients has increased.
    Beck anxiety scale
    as a result of listening to prayer for 1 month, the anxiety severity of the participants in the experimental group decreased. A minimum of 0 and a maximum of 63 points are taken from the scale. The increase in scores indicates that the frequency of anxiety of patients has increased.
    Spiritual Well-Being Scale
    as a result of listening to prayer for 1 month, the spiritual well-being levels of the participants in the experimental group increased. A minimum of 0 and a maximum of 48 points are taken from the scale. An increase in scores indicates an increase in the spiritual well-being of patients.

    Secondary Outcome Measures

    Full Information

    First Posted
    August 10, 2023
    Last Updated
    September 16, 2023
    Sponsor
    Cumhuriyet University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05997394
    Brief Title
    The Effect of Prayer on Dyspnea Severity, Anxiety and Spiritual Well-Being in Individuals With COPD
    Acronym
    COPD
    Official Title
    The Effect of Prayer on Dyspnea Severity, Anxiety and Spiritual Well-Being in Individuals With COPD
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    October 1, 2023 (Anticipated)
    Primary Completion Date
    January 1, 2024 (Anticipated)
    Study Completion Date
    May 1, 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Cumhuriyet 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
    This study will be conducted in order to examine the effect of prayer to individuals with COPD on the severity of dyspnea, anxiety and spiritual well-being experienced by patients.
    Detailed Description
    This study will be conducted on people with COPD. People with COPD disease will be divided into two groups. The experimental group will be given a prayer lesson for a month. Prayer listening will not be performed to the control group. At the end of one month, the severity of dyspnea, anxiety and spiritual well-being levels of people in both groups will be re-evaluated.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    COPD
    Keywords
    DYSPNEA, SPIRITUAL GOODNESS, ANXIETY

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    It is a semi-experimental type of study. It consists of two groups: experiment and control.
    Masking
    ParticipantInvestigator
    Masking Description
    The experimental and control groups will be determined by randomization method by a person other than the researcher. Participants will not know which group they are in.
    Allocation
    Randomized
    Enrollment
    90 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Experimental Group
    Arm Type
    Experimental
    Arm Description
    Participants in this group will be given a prayer concert for a month. At the end of one month, the severity of dyspnea, anxiety and spiritual well-being levels experienced by the participants will be re-checked.
    Arm Title
    Control Group
    Arm Type
    No Intervention
    Arm Description
    There will be no prayer audience for participants in this group.
    Intervention Type
    Other
    Intervention Name(s)
    A prayer concert will be held for the participants.
    Intervention Description
    Participants who are in the experimental group will be given a prayer audience.
    Primary Outcome Measure Information:
    Title
    dyspnea 12 scale
    Description
    as a result of 1-month prayer listening, the severity of dyspnea of the participants in the experimental group decreased. A minimum of 0 and a maximum of 36 points are taken from the scale. The increase in scores indicates that the frequency of dyspnea of patients has increased.
    Time Frame
    1 month
    Title
    Beck anxiety scale
    Description
    as a result of listening to prayer for 1 month, the anxiety severity of the participants in the experimental group decreased. A minimum of 0 and a maximum of 63 points are taken from the scale. The increase in scores indicates that the frequency of anxiety of patients has increased.
    Time Frame
    1 month
    Title
    Spiritual Well-Being Scale
    Description
    as a result of listening to prayer for 1 month, the spiritual well-being levels of the participants in the experimental group increased. A minimum of 0 and a maximum of 48 points are taken from the scale. An increase in scores indicates an increase in the spiritual well-being of patients.
    Time Frame
    1 month

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: 90 individuals (45 experiments, 45 controls) who can be contacted, who have agreed to participate in the study who are literate, can speak Turkish who have not participated in a similar application of this study before who have agreed to participate in the study after being informed about the research are 18 years old and over, with a COPD diagnosis will be taken Exclusion Criteria: Individuals with mental and hearing problems, who have lost a family member and someone close to them in the last year who are using tranquilizers/antidepressants who have experienced a traumatic situation such as divorce will be excluded from the sample.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Gülden Kaygusuz Gülden Kaygusuz
    Phone
    guldenkay.48@gmail.com
    Ext
    +905382124060
    Email
    guldenkay.48@gmail.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Gülden Kaygusuz Gülden Kaygusuz
    Organizational Affiliation
    Tokat Zile Devlet Hatanesi
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    IPD Sharing Plan Description
    It is not intended to share the data of individual participants.

    Learn more about this trial

    The Effect of Prayer on Dyspnea Severity, Anxiety and Spiritual Well-Being in Individuals With COPD

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