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PTH and Vibration in OSteoporosis Study (PaVOS)

Primary Purpose

Osteoporosis

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
whole-body vibration
teriparatide
Sponsored by
Odense University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoporosis focused on measuring whole body vibration, PTH

Eligibility Criteria

50 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Women starting PTH treatment for osteoporosis according to Danish Osteoporosis guidelines

Exclusion Criteria:

  • Women currently taking oral glucocorticoids
  • Women unable to give informed consent
  • Women unable to stand for 2 minutes at a time on the vibration platform
  • Women who have contraindications to WBV (e.g. joint prosthesis, pacemakers)

Sites / Locations

  • Odense University Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Experimental

Arm Label

controlgroup

studygroup 1

studygroup 2

Arm Description

Teriparatide, 20 microgram/day. 24 months of treatment

Teriparatide, 20 microgram/day. 24 months of treatment. 12 months of Whole-body vibration on vibration platforms.

Teriparatide, 20 microgram/day. 24 months of treatment. 24 months of Whole-body vibration on vibration platforms

Outcomes

Primary Outcome Measures

Changes in the BMD, Bone Mineral Density of hip and spine region (Hologic DXA machine)
DXA scan of hip and spine regions, BMD (g/cm^2)

Secondary Outcome Measures

Changes in the Bone microarchitecture at the tibia
HRpQCT assesses parameters of bone microarchitecture at the tibia.
Changes in the Bone microarchitecture at the radius
HRpQCT assesses parameters of bone microarchitecture at the radius.
changes in muscle mass
Full body DXA
Changes from baseline in the markers of bone resorption
CTX, sclerostin
Changes from baseline in the markers of bone formation
P1NP
Changes in Muscle strength
Measurements of muscle strength (leg extensor power)
Changes in handgrip strength
Measurements of muscle strength (handgrip strength)
Changes in Balance
Short Physical Performance Battery (SPPB)
Adherence to WBV
Self Reporting training log
Changes in physical activity
IPAQ short version
Changes in quality of life
EQ5D questionaire.
Changes in basic mobility
Time up and go test
Changes in The Falls Efficacy Scale International
FES-I

Full Information

First Posted
September 15, 2015
Last Updated
September 17, 2020
Sponsor
Odense University Hospital
Collaborators
University of Southern Denmark, Copenhagen University Hospital, Denmark, Hospital of South West Jutland, Sygehus Lillebaelt, Odense Patient Data Explorative Network, Region of Southern Denmark
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1. Study Identification

Unique Protocol Identification Number
NCT02563353
Brief Title
PTH and Vibration in OSteoporosis Study
Acronym
PaVOS
Official Title
PTH and Vibration in OSteoporosis (PaVOS) Study
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
November 2015 (Actual)
Primary Completion Date
November 2018 (Actual)
Study Completion Date
November 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Odense University Hospital
Collaborators
University of Southern Denmark, Copenhagen University Hospital, Denmark, Hospital of South West Jutland, Sygehus Lillebaelt, Odense Patient Data Explorative Network, Region of Southern Denmark

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Objective: This is a randomized controlled trial (RCT) in osteoporosis patients randomized to standard parathyroid hormone (PTH) treatment alone or to standard PTH treatment and Whole-body vibration (WBV). PTH is an effective but expensive anabolic treatment for osteoporosis. WBV stimulates muscles and bones. A combined treatment might have synergistic or additive beneficial effects on bone, reducing fracture risk making treatment more effective and cost-effective. A beneficial effect on muscles and thereby falls risk of WBV may improve fracture risk even further. If the results of this pilot study are promising then a strong case can be made for a large multi-centre RCT using strong endpoints including fractures and falls.
Detailed Description
Study Objectives To determine if WBV in addition to standard PTH treatment has a greater effect on bone mass in osteoporosis patients compared to standard PTH treatment alone. To determine if WBV in addition to standard PTH treatment has a greater effect on bone microarchitecture in osteoporosis patients compared to standard PTH treatment alone, as assessed by high resolution peripheral quantitative computed tomography (HR-pQCT). To determine if WBV in addition to standard PTH treatment has a greater effect on markers of bone formation and resorption in osteoporosis patients compared to standard PTH treatment alone. To study the effects of WBV on muscle function and balance in osteoporosis To assess the safety and adherence to WBV in osteoporotic patients Study Design: General Design This will be a multi-center randomized controlled trial (RCT) in osteoporosis patients being started on standard PTH treatment according to Danish Osteoporosis guidelines. Participants will be randomized to standard PTH treatment alone or to standard PTH treatment and WBV. Statistical Plan: Sample Size Determination The inclusion of 32 participants (16 in both groups) would give the study 80% power to detect a clinically significant additional increase of 22% with WBV (assuming a 9% increase of BMD in the PTH alone group and 11% increase in the combined PTH+WBV group, and assuming a SD of the BMD increase of 2%. Allowing for a 20% dropout rate, the plan is to include 40 participants (20 in each group). From previous research on WBV by one of the investigators (TM), statistically significant differences were found in bone formation markers and in muscle strength at 3 months between the WBV and control groups with a sample size of 35. The number of participants in the latter pilot work is reassuringly consistent with the sample size calculations. The number needed to be included is far less (34%) than the actual number of patients treated with PTH in the recruiting departments in a similar time period last year. Statistical Methods: STATA/SPSS will be used for data analysis. For the primary endpoint (BMD at 12 months) the mean percentage changes in BMD between the two groups will be compared using Analysis of Variance (ANOVA) provided the distribution is normal. For the other endpoints parametric tests will be used to assess differences in the two groups for normally distributed data and non-parametric tests for data not normally distributed. The randomization will be done online in the data capture program Red Cap. There will be created a Data dictionary that contains detailed descriptions of each variable used by the registry, including the source of the variable, and normal ranges if relevant. Information: Participants will be recruited during their attendance at the outpatient clinics. At that time the subjects will be given a full explanation of the study as well as the patient information sheet and invited to participate in the study. At an interval of not less than 24 hours, patients will be invited to consent prior to starting their PTH treatment. The information will be sufficient for subjects to make an informed decision about their participation in this study. The subject will complete and sign a consent form to indicate they are giving valid consent to participate in the trial. Withdrawal of Subjects: Patients who withdraw consent from participation in the trial will be withdrawn from the trial. This will not affect their standard medical management and not cause any adverse effect on the subject.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoporosis
Keywords
whole body vibration, PTH

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
35 (Actual)

8. Arms, Groups, and Interventions

Arm Title
controlgroup
Arm Type
Active Comparator
Arm Description
Teriparatide, 20 microgram/day. 24 months of treatment
Arm Title
studygroup 1
Arm Type
Experimental
Arm Description
Teriparatide, 20 microgram/day. 24 months of treatment. 12 months of Whole-body vibration on vibration platforms.
Arm Title
studygroup 2
Arm Type
Experimental
Arm Description
Teriparatide, 20 microgram/day. 24 months of treatment. 24 months of Whole-body vibration on vibration platforms
Intervention Type
Other
Intervention Name(s)
whole-body vibration
Other Intervention Name(s)
vibration therapy
Intervention Description
Whole-body vibration on vibration platforms. 30-40 Hertz, from 2 mm (low) to 4 mm (high) amplitude, 1 minutes x 6 with 1 minute break between. 3 times a week.
Intervention Type
Drug
Intervention Name(s)
teriparatide
Other Intervention Name(s)
PTH
Intervention Description
Teriparatide, 20 microgram/day. 24 months of treatment.
Primary Outcome Measure Information:
Title
Changes in the BMD, Bone Mineral Density of hip and spine region (Hologic DXA machine)
Description
DXA scan of hip and spine regions, BMD (g/cm^2)
Time Frame
at the time the participants start treatment and in an interval as close as possible to after 6, 12, 18, 24 months from baseline
Secondary Outcome Measure Information:
Title
Changes in the Bone microarchitecture at the tibia
Description
HRpQCT assesses parameters of bone microarchitecture at the tibia.
Time Frame
at the time the participants start treatment and in an interval as close as possible to after 6, 12, 18 and 24 months from baseline
Title
Changes in the Bone microarchitecture at the radius
Description
HRpQCT assesses parameters of bone microarchitecture at the radius.
Time Frame
at the time the participants start treatment and in an interval as close as possible to after 6, 12, 18 and 24 months from baseline
Title
changes in muscle mass
Description
Full body DXA
Time Frame
at the time the participants start treatment and in an interval as close as possible to after 12 and 24 months from baseline
Title
Changes from baseline in the markers of bone resorption
Description
CTX, sclerostin
Time Frame
at the time the participants start treatment and in an interval as close as possible to after 3, 6, 12, 18, 24 months from baseline
Title
Changes from baseline in the markers of bone formation
Description
P1NP
Time Frame
at the time the participants start treatment and in an interval as close as possible to after 3, 6, 12, 18, 24 months from baseline
Title
Changes in Muscle strength
Description
Measurements of muscle strength (leg extensor power)
Time Frame
at the time the participants start treatment and in an interval as close as possible to after 3,6,12,18 and 24 months from baseline
Title
Changes in handgrip strength
Description
Measurements of muscle strength (handgrip strength)
Time Frame
at the time the participants start treatment and in an interval as close as possible to after 3,6,12,18 and 24 months from baseline
Title
Changes in Balance
Description
Short Physical Performance Battery (SPPB)
Time Frame
at the time the participants start treatment and in an interval as close as possible to after 3, 6 ,12, 18 and 24 months from baseline
Title
Adherence to WBV
Description
Self Reporting training log
Time Frame
During 2 years from the start of the treatment
Title
Changes in physical activity
Description
IPAQ short version
Time Frame
at the time the participants start treatment and in an interval as close as possible to after 12, and 24 months from baseline
Title
Changes in quality of life
Description
EQ5D questionaire.
Time Frame
at the time the participants start treatment and in an interval as close as possible to after 12, and 24 months from baseline
Title
Changes in basic mobility
Description
Time up and go test
Time Frame
at the time the participants start treatment and in an interval as close as possible to after 3,6,12,18 and 24 months from baseline
Title
Changes in The Falls Efficacy Scale International
Description
FES-I
Time Frame
at the time the participants start treatment and in an interval as close as possible to after 12, and 24 months from baseline

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women starting PTH treatment for osteoporosis according to Danish Osteoporosis guidelines Exclusion Criteria: Women currently taking oral glucocorticoids Women unable to give informed consent Women unable to stand for 2 minutes at a time on the vibration platform Women who have contraindications to WBV (e.g. joint prosthesis, pacemakers)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lars Matzen, Clin.Ass.Pro
Organizational Affiliation
Odense University Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ditte Jepsen, MD, ph.d. student
Organizational Affiliation
University of Southern Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
Odense University Hospital
City
Odense
ZIP/Postal Code
5000
Country
Denmark

12. IPD Sharing Statement

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PTH and Vibration in OSteoporosis Study

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