COMPLETED

Fitness Integrative Training for Pediatric Rheumatology Disorders

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

This study evaluates the feasibility of the Fitness Integrative Training program for Teens (FIT Teens 2), a combined cognitive behavioral therapy and neuromuscular exercise training program in patients with pediatric rheumatic diseases and/or joint hypermobility.

Official Title

Fitness Integrative Training for Pediatric Rheumatology Disorders (FIT Teens II): a Pilot Feasibility Study

Quick Facts

Study Start:2024-09-24
Study Completion:2025-07-02
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT06556992

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:10 Years to 19 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT
Inclusion CriteriaExclusion Criteria
  1. * Pediatric rheumatic diseases (PRD) or joint hypermobility (JH) diagnosed by a pediatric rheumatologist or pain physician.
  2. * Initial diagnosis ≥ 3 months ago
  3. * Ages 10-19 years, inclusive
  4. * Ongoing symptoms of musculoskeletal pain and/or fatigue for at least 3 months
  5. * Functional Disability Index (FDI) Score ≥ 13 indicating at least moderate disability.
  6. * Child has written and spoken proficiency in English and parent has written and spoken proficiency in English or Spanish (will have a certified bilingual provider or interpreter available)
  1. * Untreated major psychiatric diagnoses (e.g., major depression, bipolar disorder, psychoses) or documented developmental delay.
  2. * Any other medical condition determined by their physician to be a contraindication for exercise.
  3. * Childhood Myositis Assessment Scale (CMAS) ≤ 30

Contacts and Locations

Principal Investigator

Susmita Kashikar-Zuck, PhD
PRINCIPAL_INVESTIGATOR
Children's Hospital Medical Center, Cincinnati

Study Locations (Sites)

Cincinnati Children's Hospital Medical Center
Cincinnati, Ohio, 45229
United States

Collaborators and Investigators

Sponsor: Children's Hospital Medical Center, Cincinnati

  • Susmita Kashikar-Zuck, PhD, PRINCIPAL_INVESTIGATOR, Children's Hospital Medical Center, Cincinnati

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 Date2024-09-24
Study Completion Date2025-07-02

Study Record Updates

Study Start Date2024-09-24
Study Completion Date2025-07-02

Terms related to this study

Additional Relevant MeSH Terms

  • Juvenile Idiopathic Arthritis
  • Systemic Lupus Erythematosus of Childhood
  • Joint Hypermobility
  • Juvenile Dermatomyositis