RECRUITING

Resilience Mobile App for Teens and Young Adults With Cancer

Conditions

Cancer Mobile health Quality of life Adolescent Young Adult Psychosocial factors

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this pilot trial is to examine whether a mobile app version of the Promoting Resilience in Stress Management (PRISM) intervention is acceptable, easy to use, and helps improve quality of life and mental health symptoms.

Official Title

Pilot Trial Testing Mobile Health Psychosocial Intervention for Adolescents and Young Adults With Cancer

Quick Facts

Study Start:2023-09-12

Study Completion:2027-08-31

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT05842902

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:12 Years to 25 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:CHILD, ADULT

Inclusion Criteria	Exclusion Criteria
* Age 12-25 years * Diagnosis of new malignancy within 12 months of enrollment treated with chemotherapy and/or radiation therapy at Seattle Children's Hospital (SCH) * Patient able to speak/read/write English or Spanish language * Cognitively able to participate in mHealth psychosocial intervention and interactive interviews	* Patient refusal to participate (any age), or parental refusal to participate for patients less than 18 years of age * Patients with diagnosis of malignancy \>12 months * Patients with relapsed, recurrent, or refractory disease * Patient without chemotherapy and/or radiation therapy as part of cancer treatment (e.g., surgical resection only patients are not-eligible) * Cognitively or physically unable to participate in mHealth psychosocial intervention and surveys

Inclusion Criteria

Exclusion Criteria

* Age 12-25 years
* Diagnosis of new malignancy within 12 months of enrollment treated with chemotherapy and/or radiation therapy at Seattle Children's Hospital (SCH)
* Patient able to speak/read/write English or Spanish language
* Cognitively able to participate in mHealth psychosocial intervention and interactive interviews

* Patient refusal to participate (any age), or parental refusal to participate for patients less than 18 years of age
* Patients with diagnosis of malignancy \>12 months
* Patients with relapsed, recurrent, or refractory disease
* Patient without chemotherapy and/or radiation therapy as part of cancer treatment (e.g., surgical resection only patients are not-eligible)
* Cognitively or physically unable to participate in mHealth psychosocial intervention and surveys

Contacts and Locations

Study Contact

Nancy Lau, PhD

CONTACT

206-884-0569

nancy.lau@seattlechildrens.org

Study Locations (Sites)

Seattle Children's Hospital

Seattle, Washington, 98105

United States

Collaborators and Investigators

Sponsor: Seattle Children's Hospital

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-09-12

Study Completion Date2027-08-31

Study Record Updates

Study Start Date2023-09-12

Study Completion Date2027-08-31

Terms related to this study

Keywords Provided by Researchers

Mobile health
Quality of life
Adolescent
Young Adult
Psychosocial factors

Additional Relevant MeSH Terms

Cancer