Osteoporosis Prevention in Preadolescent Girls
Osteoporosis Prevention in Preadolescent Girls
clinicaltrials.gov
This study has been completed.
Sponsored by: National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Information provided by: National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
ClinicalTrials.gov Identifier: NCT00000413
Purpose
This study will test an osteoporosis prevention program aimed at preadolescent girls between the ages of 10 and 12 who have not yet started their menstrual periods. Girls in this age group are adding large amounts of new bone to their skeletons. Adding more bone at this time of life can reduce a person's chances of developing osteoporosis (thinning bones) in later years.
We will look at how this osteoporosis prevention program affects the amount of calcium in the girls' diets, the amount of weight-bearing exercise they do, and their bone mass measured using ultrasound testing of the heel.
Condition Intervention Phase
Osteoporosis
Behavioral: Psychoeducational program
Phase II
MedlinePlus related topics: Exercise and Physical Fitness Osteoporosis
U.S. FDA Resources
Study Type: Interventional
Study Design: Prevention, Randomized, Single Blind, Active Control, Parallel Assignment, Efficacy Study
Official Title: Osteoporosis Prevention in Preadolescent Girls
Further study details as provided by National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS):
Estimated Enrollment: 340
Study Start Date: July 1998
Estimated Study Completion Date: June 2002
Detailed Description:
The study's objective is to demonstrate the efficacy of a behavioral/educational intervention in increasing levels of dietary calcium intake and weight-bearing exercise within an at-risk population in a stage of rapid accrual of bone mass-specifically, premenarchal girls between the ages of 10 and 12. We will use cluster randomization to randomize girls to either the intervention or a program of education only. We will randomize eighteen groups of girls into each arm of the study.
The intervention consists of six interactive sessions using various media (i.e., overhead transparencies, graphics, and three-dimensional demonstrations) to present instructional material. Topics include an explanation of osteoporosis and its modifiable and nonmodifiable risk factors, prevention of osteoporosis via healthy food choices (i.e., high calcium, low fat foods), and prevention of osteoporosis via weight-bearing exercise. Each girl monitors her own progress toward the goal of 1350 to 1500 milligrams of calcium per day. A similar method allows simple self-monitoring of weight-bearing activity. The intervention program is reinforced via monthly self-monitoring for 18 months. The education-only program consists of six generic sessions on healthy eating, physical fitness, and healthy lifestyle choices.
The primary outcomes of interest are higher calcium intake and higher levels of weight-bearing exercise. A secondary outcome of interest is increased broadband ultrasound attenuation of the os calcis, assessed using quantitative ultrasound. In summary, the group of girls targeted is ideal for this intervention because they are at a stage of rapid accrual of bone mass.
Eligibility
Ages Eligible for Study: 9 Years to 13 Years
Genders Eligible for Study: Female
Accepts Healthy Volunteers: Yes
Criteria
Inclusion Criteria:
9- and 10-year-old premenarchal girls (girls who have not started their periods).
Exclusion Criteria:
Comorbid conditions or medications that are associated with decreased bone density such as the following: corticosteroids; anticonvulsants; thiazide diuretics; history of cancer; Type I diabetes; thyrotoxicosis; hyperparathyroidism; Cushing's syndrome; juvenile rheumatoid arthritis; connective tissue disease or hemolytic anemia; asthma which may limit ability to participate in the exercise intervention; known history of dietary disorder, including anorexia, bulimia or lactose intolerance; postmenarchal.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00000413
Locations
United States, Ohio
University Hospitals of Cleveland
Cleveland, Ohio, United States, 44106
Sponsors and Collaborators
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Investigators
Principal Investigator: C. Kent Kwoh, MD Case Western Reserve Univ. and Univ. Pittsburgh
More Information
Publications:
Ievers-Landis CE, Burant C, Drotar D, Morgan L, Trapl ES, Kwoh CK. Social support, knowledge, and self-efficacy as correlates of osteoporosis preventive behaviors among preadolescent females. J Pediatr Psychol. 2003 Jul-Aug;28(5):335-45.
Study ID Numbers: P60 AR20618, NIAMS-018
Study First Received: November 3, 1999
Last Updated: December 28, 2006
ClinicalTrials.gov Identifier: NCT00000413 history of changes since first registered
Health Authority: United States: Federal Government
Keywords provided by National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS):
Osteoporosis prevention
Behavioral/educational intervention
Preadolescent
Calcium
Exercise
Peak bone mass
Bone density
Study placed in the following topic categories:
Calcium, Dietary
Musculoskeletal Diseases
Osteoporosis
Bone Diseases, Metabolic
Bone Diseases
ClinicalTrials.gov processed this record on February 11, 2009
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