Exploring the Experience of Using a Prayer Mobile App

NCT ID: NCT05626673

Last Updated: 2025-09-30

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

77 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-01-24

Study Completion Date

2023-06-19

Brief Summary

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The goal of this clinical trial is to explore the feasibility and preliminary effects of using Pray.com on spiritual well-being and mental health symptoms in racial/ethnic minority adults. The main question it aims to answer is: What are the feasibility and preliminary effects of using Pray.com on spiritual well-being and mental health (stress, depressive and anxiety symptoms) in racial ethnic minority adults (i.e., individuals who identify as Black/African American, Latinx/Hispanic, Asian/Pacific Islander, Native American, or Multiracial)?

Participants will be given the Pray.com app and directed to use it daily. Participants will complete measures at baseline (i.e., time 1) and four-weeks (i.e., time 2). A smaller subset of participants will be asked to participate in a qualitative interview.

Detailed Description

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Participants (N = 75) will be recruited through social media and various Christian organizations that serve racial/ethnic minorities. Participants will be over the age of 18 and identify as a racial/ethnic minority (i.e., individuals who identify as Black/African American, Latinx/Hispanic, Asian/Pacific Islander, Native American, or Multiracial). Participants also must be willing to participate in a study that involves engaging in a regular Christian religious practice and are willing to download the Pray.com app.

Eligible participants will be given the Pray.com app and directed to use it daily. Participants will complete measures at baseline (i.e., time 1) and four-weeks (i.e., time 2). At the end of the study participants will be randomly asked to participate in an interview (N = 15) which will take no longer than 60 minutes.

Conditions

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No Specific Condition. Feasibility of Mobile App

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Participants will be provided access to the Pray.com app and directed to use it for at least 5 minutes per day for at least 5 times per week.
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Prayer app

Participants will be given the Pray.com app and directed to use it daily.

Group Type EXPERIMENTAL

Prayer app

Intervention Type BEHAVIORAL

Participants will be given the Pray.com app and directed to use it daily.

Interventions

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Prayer app

Participants will be given the Pray.com app and directed to use it daily.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* 18 years of age or older.
* Identify as a racial/ethnic minority (e.g., Black/African American, Latinx/Hispanic, Asian/Pacific Islander, Native American, Multiracial).
* Own a smart phone and be willing to download a mobile app.
* Willing to engage in a Christian-based religious practice on a mobile app.

Exclusion Criteria

* n/a
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Biola University

OTHER

Sponsor Role lead

Responsible Party

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Todd Hall

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Todd Hall, PhD

Role: PRINCIPAL_INVESTIGATOR

Biola University

Locations

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Biola University

La Mirada, California, United States

Site Status

Countries

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United States

Provided Documents

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Document Type: Study Protocol, Statistical Analysis Plan, and Informed Consent Form

View Document

Other Identifiers

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F22-013

Identifier Type: -

Identifier Source: org_study_id

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