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Bone Health in Pediatric Crohn's Disease: A Low Magnitude Mechanical Stimulus Trial

Primary Purpose

Crohn Disease

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Low magnitude mechanical stimulus
Placebo (inactive) low magnitude mechanical stimulus
Sponsored by
Children's Hospital of Philadelphia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Crohn Disease

Eligibility Criteria

8 Years - 21 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age 8-21 years Diagnosis of Crohn disease > 6 months Tibia vBMD z-score < 25th%tile for age and sex Exclusion Criteria: Pregnancy Weight > 250 lb Medical illness (unrelated to Crohn) Cognitive/developmental disorder Do not speak English > 1 primary residence Unwilling to commit to 2 year study Sibling or cousin enrolled in trial

Sites / Locations

  • The Children's Hospital of Philadelphia

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Active Low Magnitude Mechanical Stimulus

Inactive Low Magnitude mechanical Stimulus

Arm Description

Active Low Magnitude Mechanical Stimulus

Inactive, or placebo low magnitude mechanical stimulus

Outcomes

Primary Outcome Measures

Change in Tibia Trabecular Volumetric Bone Mineral Density (BMD) Z-score at 12 Months
We calculated the mean change in tibia trabecular volumetric BMD Z-score between baseline and 12 months, as measured by peripheral quantitative computed tomography (pQCT). The Z-score, or Standard Deviation Score, is a measure of the number of standard deviations that an individual is above or below the median value in a healthy child or adolescent of the same age, sex and race. For example, a Z-score of 0 means that an individual's result is equivalent to the 50th percentile in a healthy population. A Z-score of -1.0 means that an individual's result is equovalent to the 16th percentile in a healthy population.
Change in Tibia Cortical Area Z-score 12 Months
We calculated the mean change in tibia cortical area Z-score, as measured by pQCT, between baseline and 12 months.
Change in Spine Volumetric BMD Z-score at 12 Months
We calculated the mean change in spine volumetric BMD Z-score, as measured by QCT, between baseline and 12 months

Secondary Outcome Measures

Change in Posteroanterior Lumbar Spine Areal BMD Z-score
We calculated the mean change in posterior anterior lumbar spine areal BMD Z-score between baseline and 12 months as measured by DXA
Change in Total Hip Areal BMD Z-score Between Baseline and 12 Months
We calculated the mean change in total hip bone mineral density z-score, as measured by DXA, between baseline and 12 months
Change in Femoral Neck Areal BMD Z-score Between Baseline and 12 Months
We calculated the mean change in femoral neck areal bmd Z-score between baseline and 12 months as measured by DXA
Change in Whole Body Bone Mineral Content Z-score Between Baseline and 12 Months
We calculated the mean change in whole body bone mineral content Z-score, as measured by DXA, between baseline and 12 months
Change in QCT Tibia Trabecular Volumetric BMD at 12 Months
We calculated the mean change in tibia trabecular volumetric BMDbetween baseline and 12 months as measured by (QCT)

Full Information

First Posted
August 14, 2006
Last Updated
March 17, 2017
Sponsor
Children's Hospital of Philadelphia
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
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1. Study Identification

Unique Protocol Identification Number
NCT00364130
Brief Title
Bone Health in Pediatric Crohn's Disease: A Low Magnitude Mechanical Stimulus Trial
Official Title
Bone Health in Pediatric Crohn's Disease: A Low Magnitude Mechanical Stimulus Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2017
Overall Recruitment Status
Completed
Study Start Date
February 2007 (undefined)
Primary Completion Date
August 2012 (Actual)
Study Completion Date
August 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Children's Hospital of Philadelphia
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this 12-month double blind, placebo controlled randomized trial is to evaluate the effects of daily treatments with low magnitude mechanical stimuli on bone in 160 children with Crohn disease.
Detailed Description
Skeletal growth is characterized by increases in the size of the hard outer layer of bone (cortical bone), and the density of the inner layer of bone (trabecular or "spongy" bone). Children with Crohn disease (CD) have numerous risk factors for impaired bone accumulation, including poor growth, delayed puberty, malnutrition, glucocorticoid therapy and inflammation. We reported that children with CD had significant deficits in trabecular bone mineral density (BMD), cortical dimensions, and muscle mass; bone deficits were strongly associated with muscle deficits. No trials of therapies that build bone or prevent bone breakdown have been conducted in chronic pediatric inflammatory diseases. The capacity to increase bone mass and dimensions in response to mechanical loading is greatest during growth. Recent studies demonstrate that brief daily exposure to low magnitude mechanical stimuli (LMMS) enhances bone mass and quality. This 12-month double blind, placebo controlled randomized trial will evaluate daily 10-minute treatments with LMMS in 160 children with CD. Trabecular BMD, cortical dimensions, and muscle area will be measured by quantitative computed tomography (QCT). The LMMS device monitors adherence; these data will be transmitted by modem to the psychologist who will work closely with subjects to optimize adherence. All subjects will be provided with calcium and vitamin D supplements. The primary aims are to determine if treatment with LMMS results in increased trabecular BMD in the lower leg and spine and increased cortical dimensions in the lower leg in children with CD, compared with placebo controls.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Crohn Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
138 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Active Low Magnitude Mechanical Stimulus
Arm Type
Active Comparator
Arm Description
Active Low Magnitude Mechanical Stimulus
Arm Title
Inactive Low Magnitude mechanical Stimulus
Arm Type
Placebo Comparator
Arm Description
Inactive, or placebo low magnitude mechanical stimulus
Intervention Type
Device
Intervention Name(s)
Low magnitude mechanical stimulus
Other Intervention Name(s)
Whole body vibration
Intervention Description
10 minute daily treatment sessions standing on the low magnitude mechanical stimulus device
Intervention Type
Device
Intervention Name(s)
Placebo (inactive) low magnitude mechanical stimulus
Intervention Description
10 minute daily treatments standing on a placebo version of a low magnitude mechanical stimulus device
Primary Outcome Measure Information:
Title
Change in Tibia Trabecular Volumetric Bone Mineral Density (BMD) Z-score at 12 Months
Description
We calculated the mean change in tibia trabecular volumetric BMD Z-score between baseline and 12 months, as measured by peripheral quantitative computed tomography (pQCT). The Z-score, or Standard Deviation Score, is a measure of the number of standard deviations that an individual is above or below the median value in a healthy child or adolescent of the same age, sex and race. For example, a Z-score of 0 means that an individual's result is equivalent to the 50th percentile in a healthy population. A Z-score of -1.0 means that an individual's result is equovalent to the 16th percentile in a healthy population.
Time Frame
12 months
Title
Change in Tibia Cortical Area Z-score 12 Months
Description
We calculated the mean change in tibia cortical area Z-score, as measured by pQCT, between baseline and 12 months.
Time Frame
12 months
Title
Change in Spine Volumetric BMD Z-score at 12 Months
Description
We calculated the mean change in spine volumetric BMD Z-score, as measured by QCT, between baseline and 12 months
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Change in Posteroanterior Lumbar Spine Areal BMD Z-score
Description
We calculated the mean change in posterior anterior lumbar spine areal BMD Z-score between baseline and 12 months as measured by DXA
Time Frame
12 months
Title
Change in Total Hip Areal BMD Z-score Between Baseline and 12 Months
Description
We calculated the mean change in total hip bone mineral density z-score, as measured by DXA, between baseline and 12 months
Time Frame
12months
Title
Change in Femoral Neck Areal BMD Z-score Between Baseline and 12 Months
Description
We calculated the mean change in femoral neck areal bmd Z-score between baseline and 12 months as measured by DXA
Time Frame
12 months
Title
Change in Whole Body Bone Mineral Content Z-score Between Baseline and 12 Months
Description
We calculated the mean change in whole body bone mineral content Z-score, as measured by DXA, between baseline and 12 months
Time Frame
12 months
Title
Change in QCT Tibia Trabecular Volumetric BMD at 12 Months
Description
We calculated the mean change in tibia trabecular volumetric BMDbetween baseline and 12 months as measured by (QCT)
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
8 Years
Maximum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 8-21 years Diagnosis of Crohn disease > 6 months Tibia vBMD z-score < 25th%tile for age and sex Exclusion Criteria: Pregnancy Weight > 250 lb Medical illness (unrelated to Crohn) Cognitive/developmental disorder Do not speak English > 1 primary residence Unwilling to commit to 2 year study Sibling or cousin enrolled in trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Babette Zemel, MD
Organizational Affiliation
Children's Hospital of Philadelphia
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Children's Hospital of Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States

12. IPD Sharing Statement

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Bone Health in Pediatric Crohn's Disease: A Low Magnitude Mechanical Stimulus Trial

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