Mobile Coach for Parents of Children and Adolescents With Chronic Pain

NCT ID: NCT03356275

Last Updated: 2018-04-12

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

34 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-12-18

Study Completion Date

2018-03-13

Brief Summary

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Chronic pain is estimated to affect 20% to 35% of children and adolescents around the world, and is associated with increased risk of anxiety and depression among children and adolescents, as well as coping challenges, anxiety, depression, and anger in their parents. For parents, learning to manage stress is critical, as parents play a significant role in a child's experience of pain. Parental behaviors such as over-involvement, solicitousness and rejection are associated with decreased functioning, including higher school absenteeism in children and teens. A number of interventions demonstrate that teaching skills to parents can have a direct and positive impact on the health of children and adolescents with chronic pain. The investigators propose to create and test the BodiMojo Parent Buddy which will provide parents with real-time, tailored and adaptive coping and stress management support and will provide a curriculum of skills for responding to a child in pain in order to promote child functioning.

Thirty parents of children ages 8-18 who have been diagnosed with a non-cancer chronic pain condition will participate in this user-testing study. Parents will complete a brief set of questionnaires before and after the intervention, and will be instructed to open and use the app each day for 30 days. Participants will complete audio mindfulness exercises, watch brief video clips, and read psychoeducational information about pain, coping, and communication skills. Post-intervention questionnaires will also include an acceptance test to assess participants' opinions about the helpfulness and usability of the app. Parent participation is expected to take around 3.5 hours total over the 30 day study period.

Detailed Description

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Conditions

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Parents Chronic Pain Pediatric Disorder

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Mobile application

Psychosocial support for parents, including: brief audio mindfulness recordings, videos, and psychoeducational materials.

Group Type EXPERIMENTAL

Mindfulness for Resilience in Illness: Support for Parents

Intervention Type BEHAVIORAL

Mobile application focusing on emotional coping skills for parents of children and adolescents with chronic pain. Components of the module include: library of mindfulness meditations/relaxations; peer support videos; and psychoeducational information related to pain, stress, and mindfulness.

Interventions

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Mindfulness for Resilience in Illness: Support for Parents

Mobile application focusing on emotional coping skills for parents of children and adolescents with chronic pain. Components of the module include: library of mindfulness meditations/relaxations; peer support videos; and psychoeducational information related to pain, stress, and mindfulness.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Parents who self-report parenting a child or adolescent ages 8-18 with non-cancer chronic pain.
* Daily use of a smartphone (iOS, Android, or Windows) or tablet.
* Ability to speak and understand English.

Exclusion Criteria

* Inability to provide consent
* Inability to speak and understand English
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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BodiMojo, Inc.

OTHER

Sponsor Role collaborator

University of California, Los Angeles

OTHER

Sponsor Role lead

Responsible Party

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Lonnie Zeltzer

Distinguished Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Lonnie K Zeltzer, MD

Role: PRINCIPAL_INVESTIGATOR

University of California, Los Angeles

Locations

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UCLA Pediatric Pain and Palliative Care Program Research Offices

Los Angeles, California, United States

Site Status

Countries

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United States

Other Identifiers

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R43HD090774

Identifier Type: NIH

Identifier Source: org_study_id

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