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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

90 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-01-10

Study Completion Date

2024-05-04

Brief Summary

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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.

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Detailed Description

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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.

Conditions

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COPD

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

It is a semi-experimental type of study. It consists of two groups: experiment and control.

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

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.

Study Groups

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Experimental Group

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.

Group Type EXPERIMENTAL

A prayer concert will be held for the participants.

Intervention Type OTHER

Participants who are in the experimental group will be given a prayer audience.

Control Group

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

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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A prayer concert will be held for the participants.

Participants who are in the experimental group will be given a prayer audience.

Intervention Type OTHER

Eligibility Criteria

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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.

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No