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Psychology Mobile Apps for Parents in a Pandemic

Primary Purpose

Stress, Psychological

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Mindfulness
Gratitude
Food Journal
Sponsored by
Sam Houston State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Stress, Psychological focused on measuring Parental stress, Health Psychology, Mental health apps, Mindfulness, Gratitude

Eligibility Criteria

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

Inclusion Criteria:

  1. Only individuals aged 18 and older will be allowed to participate in the current research (assessed by participant self-report).
  2. Individuals must identify oneself as a parent or primary caregiver of a child/children aged 10 or under (assessed by participant self-report).
  3. Participants who score 30 or higher in the Parent Stress Scale (PSS) measure.
  4. Participants who reside in the U.S. and can understand and answer surveys in English.

Exclusion Criteria:

  1. Individuals under 18
  2. Non-English-speaking individuals
  3. Individuals who do not consent to the survey.
  4. Individuals who do not identify oneself as a parent or primary caregiver of a child/children under the age of 10 (assessed by participant self-report).
  5. Individuals who score 30 or lower in the PSS measure.
  6. Individuals who do not reside in the U.S.

Sites / Locations

  • Sam Houston State University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Mindfulness

Gratitude

Control

Arm Description

Participants will be asked to use the app Mindfulness Coach 10 minutes for 14 days.

Participants will be asked to use the app Grateful 10 minutes for 14 days.

Participants will be asked to use the app Day One daily for 10 minutes. Participants will be writing a daily journal entry describing what they ate during the previous day for 14 days.

Outcomes

Primary Outcome Measures

Parental Stress Scale Total Score
Parental stress will be measured with The Parental Stress Scale, an 18-item self report scale; scores range from 18-90.

Secondary Outcome Measures

Five Facet Questionnaire: Short Form Total Score
Trait mindfulness will be measured with the Five Facet Questionnaire: Short Form, a 15-item self-report scale; scores range from 15-75.
Gratitude Questionnaire-6 Total Score
Trait gratitude will be measured with the Gratitude Questionnaire-6 (GQ-6), a 6-item self-report measure that ranges from 6-42.
Gratitude Resentment and Appreciation Test-Revised Short Form Total Score
Trait gratitude will be measured with Gratitude Resentment and Appreciation Test-Revised Short Form (GRAT-R-SF), a 16-item self-report measure with scores ranging from 16-144.
Dyadic Adjustment Scale Total Score
Perceptions of one's relationship with an intimate partner will be measured via the Dyadic Adjustment Scale (DAS-7), a 7-item self-report measure with scores ranging from 0-36.
Positive & Negative Affect Scores
Positive and negative affect will be measured using the Positive and Negative Affect Schedule (PANAS), a 20-item self-report measure with PA scores ranging from 0-50 and NA scores ranging from 0-50.
Child-Parent Relationship Scale Closeness & Conflict Scores
Parents' views of their relationship with their child will be measured with the Child-Parent Relationship Scale, a 15-item self-report measure, with 7 items assessing closeness (range 7-35) and 8 items assessing conflict (range 8-40).
Perceived Stress Scale Total Score
Perceived stress will be measuring using the Perceived Stress Scale (PSS), a 10-item self-report measure with scores ranging from 0-40.

Full Information

First Posted
July 19, 2021
Last Updated
October 24, 2022
Sponsor
Sam Houston State University
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1. Study Identification

Unique Protocol Identification Number
NCT04980365
Brief Title
Psychology Mobile Apps for Parents in a Pandemic
Official Title
Psychology Mobile Apps for Parents in a Pandemic
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Completed
Study Start Date
June 8, 2021 (Actual)
Primary Completion Date
June 30, 2022 (Actual)
Study Completion Date
June 30, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sam Houston State 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
The purpose of this study is to determine whether parents of young children (aged 10 and under) think it is feasible (in other words, doable) and acceptable (in other words, satisfactory) to use a mobile app designed to provide personalized education and enrichment for 10 minutes/day for 14 days. The investigators hope to learn if it is reasonable to ask parents to use one of three different apps and if parents are satisfied with their participation in the study. If so, the investigators can continue to study the effect of these apps on parents' stress in future research. The investigators also plan to evaluate the effect of these app-based interventions in lowering levels of stress in parents during the COVID-19 pandemic. By conducting this study, the investigators hope to learn if there are specific app-based interventions that will lead to a reduction in stress in parents, improved parental life satisfaction, and improved parent-child interactions. If the results of this study suggest these apps may be promising at reducing stress among parents, the investigators will continue doing research on these app-based interventions.
Detailed Description
Parents will be invited to participate in a research study to see what parents of young children (aged 10 and under) think of using one of three different mobile app-based interventions to improve parental life satisfaction. The study will be conducted by Dr. Chelsea Ratcliff and Dr. Hillary Langley, Assistant Professors of Psychology at Sam Houston State University. In addition to learning about parents' satisfaction with these app-based interventions, the investigators also plan to compare the effect of these app-based interventions on levels of parental stress, and on quality of parent-child interactions during the COVID-19 pandemic. The purpose of this research is to learn if it is reasonable to ask parents to use one of three different apps and if parents are satisfied with their participation in the study. If so, the investigators can continue to study the effect of these apps. The investigators also plan to evaluate the effect of these app-based interventions in lowering levels of stress in parents. By conducting this study, the investigators hope to learn if there are specific app-based interventions that will lead to a reduction in stress in parents, improved parental life satisfaction, and improved parent-child interactions. In order to be eligible to participate, participants must be 18 years old or older, and a parent or primary caregiver of a child/children aged 10 years or young. Participants will first consent to participate by signing their name electronically using the mouse at the end of this consent form and providing their name and email address so the investigators can maintain contact. After reading this consent form and agreeing to it, participants will be directed to complete the first survey, which will take about 30 minutes to complete. They will be asked to complete two short questionnaires to determine their eligibility for the study. Participants will receive a $5 gift card for completing the first questionnaire. After completing the pre-intervention survey, participants will be randomly assigned to use one of three psychology mobile apps. The study coordinator will email them to set up a 15-minute Zoom meeting in order to provide more information about the intervention and to help download the app that they were assigned. After the 14-day period, the study coordinator will email participants a link to a 20-minute follow-up survey, and they will receive a $5 gift card for completing this survey. One month later, the study coordinator will email participants a link to the final follow-up survey, and you will receive a $10 gift card for completing this survey. Thus, participants can earn up to $20 in Amazon gift cards for participating in this study ($5 for the pre-intervention survey, $5 for the immediate post-intervention survey, and $10 for the one-month post-intervention survey).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stress, Psychological
Keywords
Parental stress, Health Psychology, Mental health apps, Mindfulness, Gratitude

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Model Description
Potential participants will be provided access to an informed consent form and baseline survey via Qualtrics. After baseline is completed and eligibility confirmed, the study coordinator will randomly assign the participant to one of three app-based intervention conditions: Gratitude, Mindfulness, or control group. Next, the study coordinator will email them to schedule a Zoom meeting. The meeting will last 15 minutes and participants will be informed of what app they will use. After a 14-day period, the study coordinator will send participants a follow-up survey, and a final follow-up Qualtrics survey one month after the intervention ends. Participants will receive $5 for completing the baseline questionnaire, $5 for the immediate post-survey, and $10 for the one-month follow-up survey (participants can receive up to $20). Participants recruited via PeRP will receive one credit for completing the baseline questionnaire, two for the post-survey, and one for the follow-up.
Masking
Participant
Masking Description
Participants will have knowledge of the intervention they will receive but will have no knowledge of the other interventions used in the study.
Allocation
Randomized
Enrollment
224 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Mindfulness
Arm Type
Experimental
Arm Description
Participants will be asked to use the app Mindfulness Coach 10 minutes for 14 days.
Arm Title
Gratitude
Arm Type
Experimental
Arm Description
Participants will be asked to use the app Grateful 10 minutes for 14 days.
Arm Title
Control
Arm Type
Active Comparator
Arm Description
Participants will be asked to use the app Day One daily for 10 minutes. Participants will be writing a daily journal entry describing what they ate during the previous day for 14 days.
Intervention Type
Behavioral
Intervention Name(s)
Mindfulness
Intervention Description
Participants will be asked to use the app Mindfulness Coach daily for 10 minutes. Participants will follow app instructions for brief guided meditation sessions for 14 days.
Intervention Type
Behavioral
Intervention Name(s)
Gratitude
Intervention Description
Participants will be asked to use the app Grateful daily for 10 minutes. Participants will follow app instructions and will be answering to prompts related to gratitude provided by the app daily, for 10 minutes for 14 days.
Intervention Type
Behavioral
Intervention Name(s)
Food Journal
Intervention Description
Participants will be asked to use the app Day One daily for 10 minutes. Participants will be writing a daily journal entry describing what they ate during the previous day for 14 days.
Primary Outcome Measure Information:
Title
Parental Stress Scale Total Score
Description
Parental stress will be measured with The Parental Stress Scale, an 18-item self report scale; scores range from 18-90.
Time Frame
T1 (before intervention); T2 (immediately after intervention); T3 (1-month after intervention)
Secondary Outcome Measure Information:
Title
Five Facet Questionnaire: Short Form Total Score
Description
Trait mindfulness will be measured with the Five Facet Questionnaire: Short Form, a 15-item self-report scale; scores range from 15-75.
Time Frame
T1 (before intervention); T2 (immediately after intervention); T3 (1-month after intervention)
Title
Gratitude Questionnaire-6 Total Score
Description
Trait gratitude will be measured with the Gratitude Questionnaire-6 (GQ-6), a 6-item self-report measure that ranges from 6-42.
Time Frame
T1 (before intervention); T2 (immediately after intervention); T3 (1-month after intervention)
Title
Gratitude Resentment and Appreciation Test-Revised Short Form Total Score
Description
Trait gratitude will be measured with Gratitude Resentment and Appreciation Test-Revised Short Form (GRAT-R-SF), a 16-item self-report measure with scores ranging from 16-144.
Time Frame
T1 (before intervention); T2 (immediately after intervention); T3 (1-month after intervention)
Title
Dyadic Adjustment Scale Total Score
Description
Perceptions of one's relationship with an intimate partner will be measured via the Dyadic Adjustment Scale (DAS-7), a 7-item self-report measure with scores ranging from 0-36.
Time Frame
T1 (before intervention); T2 (immediately after intervention); T3 (1-month after intervention)
Title
Positive & Negative Affect Scores
Description
Positive and negative affect will be measured using the Positive and Negative Affect Schedule (PANAS), a 20-item self-report measure with PA scores ranging from 0-50 and NA scores ranging from 0-50.
Time Frame
T1 (before intervention); T2 (immediately after intervention); T3 (1-month after intervention)
Title
Child-Parent Relationship Scale Closeness & Conflict Scores
Description
Parents' views of their relationship with their child will be measured with the Child-Parent Relationship Scale, a 15-item self-report measure, with 7 items assessing closeness (range 7-35) and 8 items assessing conflict (range 8-40).
Time Frame
T1 (before intervention); T2 (immediately after intervention); T3 (1-month after intervention)
Title
Perceived Stress Scale Total Score
Description
Perceived stress will be measuring using the Perceived Stress Scale (PSS), a 10-item self-report measure with scores ranging from 0-40.
Time Frame
T1 (before intervention); T2 (immediately after intervention); T3 (1-month after intervention)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Only individuals aged 18 and older will be allowed to participate in the current research (assessed by participant self-report). Individuals must identify oneself as a parent or primary caregiver of a child/children aged 10 or under (assessed by participant self-report). Participants who score 30 or higher in the Parent Stress Scale (PSS) measure. Participants who reside in the U.S. and can understand and answer surveys in English. Exclusion Criteria: Individuals under 18 Non-English-speaking individuals Individuals who do not consent to the survey. Individuals who do not identify oneself as a parent or primary caregiver of a child/children under the age of 10 (assessed by participant self-report). Individuals who score 30 or lower in the PSS measure. Individuals who do not reside in the U.S.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chelsea G Ratcliff, Ph.D.
Organizational Affiliation
Sam Houston State University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sam Houston State University
City
Huntsville
State/Province
Texas
ZIP/Postal Code
77341
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
At this time, there is no plan to share individual participant data with other researchers.

Learn more about this trial

Psychology Mobile Apps for Parents in a Pandemic

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