- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03771001
5Minutes4Myself: A Wellness Program for Caregivers
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study is designed to:
- Conduct focus groups with caregivers of autistic children to understand specific stressors that they experience;
- Gather baseline data including surveys of health and well-being;
- Administer an individualized wellness program by using motivational interviews (MI) to individually tailor the program for each participant, train participants to use an app designed to support the adoption of lifestyle changes;
- Coach participants over the 4-6 months of their program; and
- Assess the usability of the app and the impact of the wellness program on caregiver's health and well-being.
Participants will be invited to the University of Wisconsin-Madison campus or participate online where they will:
- complete baseline surveys of physical and mental health, mindfulness, stress, and wellbeing (Center for Epidemiology Depression Scale -Revised; Five Facet Mindfulness Questionnaire; Perceived Stress Scale; Psychological Well-being Scale; Rand Short Form-36),
- get introduced to the study procedures and research team (Principal Investigator, Researcher, and MI-trained Masters-level occupational therapy and counseling graduate students); and
- participate in focus groups to introduce the 5Minutes4Myself program, offer data on current lifestyles, and receive training on how to use the app
Participants will be assigned coaches. They will work together in an initial lifestyle coaching session and continue meeting monthly for 4-6 months. To assess the fidelity of the coaching sessions, motivation interviewing sessions (initial and monthly) will be audio-- or video--taped to assess fidelity via the Motivational Interviewing Treatment Integrity tool (MITI). Participants will be asked to complete an assessment of their satisfaction with the coaching. Data will be archived for the ongoing project.
The coaches will use Motivational Interviewing strategies to identify barriers to implementing the mindfulness program, foster commitment talk, and elicit the participant's strategy for implementing the mindfulness program in their daily life. Participants may request additional consultation through the weekly app goal check-in or via email.
The app will host all baseline surveys allowing them to be completed electronically. The baseline surveys will be completed prior to the first coaching session. The app will also be used as a "habit builder" providing personalized notifications as to when a goal activity will be created, will have goal check ins for each goal, and will collect usage data for audio mindfulness podcasts that are part of the program. Usage data will show how often and for how long participants listened to a podcast during the intervention.
After completing the 4-6 month intervention, participants will return for another workshop that will include:
- Completion of Focus Group;
- Re-administration of 'baseline' surveys (now considered 'post-intervention');
- Assessing the usability of the app via the MSUS; and
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Wisconsin
-
Madison, Wisconsin, United States, 53706
- Community Sites
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Primary caregivers for child with autism OR primary caregiver of grandchild
- Child cared for is between 8 - 21 for caregivers of children with autism and 5-21 years of age for grandchildren being parented by grandparents
- Willingness to commit sufficient time to participate in the program
- Desire to participate in a lifestyle/wellness program
Exclusion Criteria:
- Caregivers of children younger than 8 years of age or older than 21 years of age for sample of parents of children with autism and Caregiver of child younger than 5 or older than 21 for grandparents parenting grandchildren
- Caregivers with significant mental illness (except for those diagnosed or treated for depression who will be included)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Convenience sample participants
In this feasibility study all participants will receive the intervention.
|
Coaches will use a manualized motivational interviewing approach and participants' wellness promoting changes will be supported via a habit building app that also delivers a micro-mindfulness program
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
SF-36 Questionnaire
Time Frame: Up to 6 months
|
Survey assessing mental and physical health
|
Up to 6 months
|
|
Perceived Stress Scale
Time Frame: Up to 6 months
|
The Perceived Stress Scale is a measure of the degree to which the participant perceives their life as stressful.
A series of 10 questions are asked to which the participant answers either: 0 = Never; 1 = Almost Never; 2 = Sometimes; 3 = Fairly Often; 4 = Very Often.
The scoring for positively worded questions is calculated by reversing the response (0=4, 1=3, 2=2, 3=1, 4=0).
Higher total scores indicate more perceived stress.
|
Up to 6 months
|
|
Ryff's Psychological Well-Being Scale
Time Frame: Up to 6 months
|
Ryff's Psychological Well-Being is a self-reported scale to assess well-being.
Participants respond to various statements about autonomy, environmental mastery, personal growth, positive relations with others, purpose in life, and self-acceptance and indicate how true each statement is of them on a 6-point Likert scale.
Higher scores are representative of greater sense of well-being.
|
Up to 6 months
|
|
Center for Epidemiological Depression Scale-Revised
Time Frame: Up to 6 months
|
The Center for Epidemiological Depression Scale (Revised; CESD-R) is a self-reported assessment where the participant answers 20 questions about how they have felt or behaved over the past 1-2 weeks.
It is scored: 0 = Not at All or less than 1 day; 1 = 1-2 days; 2 = 3-4 days; 3 = 5-7 days; 4 = nearly every 5 for 2 weeks.
Higher scores indicate greater depressive state.
|
Up to 6 months
|
|
Five facets of Mindfulness Questionnaire
Time Frame: Up to 6 months
|
Assess degree of mindfulness
|
Up to 6 months
|
|
Modified System Usability Scale
Time Frame: Up to 6 months
|
The Modified System Usability Scale is a 10 item questionnaire where the participants have 5 responses ranging from Strongly Agree to Strongly Disagree.
The responses are assigned values such that the total score ranges from 1-100 with higher scores indicating increased usability.
|
Up to 6 months
|
|
Participant Feedback
Time Frame: Up to 6 months
|
An important outcome measure will be direct participant feedback.
Program feedback will be collected via focus group participation.
|
Up to 6 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Elizabeth Larson, PhD, University of Wisconsin, Madison
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2015-1004
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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