Effect of Aerobic Exercise Paired With Strength Conditioning on Bone Health in Patients With Thalassemia

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to determine if a weight bearing exercise intervention can improve body composition and bone health in adolescents and adults with Thalassemia. The main questions it aims to answer are: * Does participation in a 12-week weight bearing exercise intervention change total body lean mass and percentage body fat (as assessed by DXA) in adolescents and adults with Thalassemia? * Does participation in a 12-week weight bearing exercise intervention change muscle function (assessed by hand grip strength, sit to stand and vertical jump) and endurance (assessed by the 6 minute walk test) in adolescents and adults with Thalassemia? * Does participation in a 36 week weight bearing exercise intervention (30 min/day; 5x/week) change bone mineral density as assessed by DXA in adolescents and adults with Thalassemia? Researchers will compare participants' change in body composition, muscle mass, and muscle function during a Usual Activity period (12 weeks) with an exercise intervention (Period 1: 12 weeks) to see if exercise can improve body composition and muscle function. The intervention will then be extended an additional 24 weeks for a total of 36 weeks of exercise (Period 2) to explore the change in bone mineral density between between Usual Activity and Exercise Intervention (Period 2) in individuals with Thalassemia. During the intervention period, participants will engage in a self-directed exercise regime of either weight bearing aerobic exercise or strength training exercises (30 min/day; 5x/week).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 14
Maximum Age: 40
Healthy Volunteers: f
View:

• Age: 14 - 40 years

• BMD Z-score at any skeletal site \< -1.0

• Diagnosed with thalassemia (any genotype, regardless of transfusion dependency)

• Vitamin D (25-Hydroxy) drawn within the previous 12 months \>20 ng/mL

• English speaking, able to consent

Locations
United States
California
UCSF Benioff Children's Hospital Oakland
RECRUITING
Oakland
University of California, San Francisco
RECRUITING
Oakland
Contact Information
Primary
Ellen Fung, PhD
ellen.fung@ucsf.edu
510-428-3885
Backup
Raquel Manzo, BS
raquel.manzo@ucsf.edu
510-428-3429
Time Frame
Start Date: 2024-12-01
Estimated Completion Date: 2026-06-30
Participants
Target number of participants: 20
Treatments
Other: Usual Activity
Subjects will participate in usual daily activities during this period
Sponsors
Leads: University of California, San Francisco

This content was sourced from clinicaltrials.gov