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Search Results Within Category "Children's Health"

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2 Study Matches

Heuristic Tool To Improve Symptom Self-Management in Adolescents and Young Adults With Cancer

Grace Hodges - hodgesg@vcu.edu

NCT05958316
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Inclusion Criteria:
* Has received at least 1 cycle of cancer treatment and is within 3 months of receiving that first cycle of treatment * Receiving regularly scheduled cancer treatment and will be receiving at least three more cycles * Reports at least 1 symptom related to cancer and/or its treatment * Able to speak, read, and write English as required for completion of the C-SCAT and study measures
Exclusion Criteria:
\- Cognitive and/or physical inability to complete study measures.
BEHAVIORAL: Computerized Symptom Capture Tool (C-SCAT) Intervention, BEHAVIORAL: Usual Care Control
Symptoms and Signs, Cancer, Childhood Cancer
Supportive Care, Symptom Management
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Study Locations

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Location Contacts
Children's Mercy Hospital Kansas City, Missouri Kristin Stegenga - (kstegenga@cmh.edu)
Seattle Children's Hospital @ University of Washington Seattle, Washington
University of Utah Huntsman Cancer Institute (HCI) Salt Lake City, Utah Lauri Linder - (lauri.linder@nurs.utah.edu)
University of Utah Primary Children's Hospital Salt Lake City, Utah Lauri Linder - (lauri.linder@nurs.utah.edu)
Virginia Commonwealth University Richmond, Virginia Grace Hodges - (rkelswic@vcu.edu)

Virtual Housecalls: Redesigning Pediatric Primary Care Adolescent Obesity Treatment (VHC)

Sarah M Farthing, MS - sarah.malone@vcuhealth.org

NCT07246603
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Adolescent
Inclusion Criteria:
* English or Spanish-speaking * 12-15 years of age * Receiving care at a participating clinic * Body Mass Index (BMI) ≥95% and \<120% of the 95% * Access to a mobile device with a webcam that can receive texts Parent
Inclusion Criteria:
* English or Spanish-speaking * Primary legal guardian ≥18 years of age living with the adolescent
Exclusion Criteria:
* conflicts that would inhibit the ability to participate in all aspects of the study as outlined in the study protocol * family plans to move outside of the study area or plans to no longer be a patient at a participating clinic in the 12 month study period * the primary care provider or PI determines that the study is not clinically or medically appropriate (e.g., significant psychiatric, cognitive, physical or developmental conditions that would impair their ability to complete assessments, participate in study sessions, or conduct physical activity) based on screening at study onset * adolescent exhibits severe dietary restriction or compensatory behavior (e.g., vomiting, laxative abuse) based on screening at study onset and clinical interview by a study psychologist * adolescent is currently pregnant/plans to become pregnant during study period * adolescent is participating in another weight loss program, has had or plans to undergo weight loss surgery * adolescent has a chronic medical condition(s) and/or uses medication that substantially impacts or interferes with growth, appetite, weight or physical activity participation * adolescents taking anti-obesity medication are ineligible if they are not a stable dose for at least 3 months prior to study participation
BEHAVIORAL: Virtual Housecalls
Class I Obesity, Pediatric Obesity
Lifestyle Intervention
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Study Locations

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Location Contacts
Children's Hospital of Richmond at VCU Healthy Lifestyles Center Henrico, Virginia Sarah M Farthing, MS - (sarah.malone@vcuhealth.org) Melanie K Bean, Ph.D. - (melanie.bean@vcuhealth.org)