Osteoporosis Clinical Trial
— PaVOSOfficial title:
PTH and Vibration in OSteoporosis (PaVOS) Study
NCT number | NCT02563353 |
Other study ID # | S-20150121 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | November 2015 |
Est. completion date | November 2019 |
Verified date | September 2020 |
Source | Odense University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 35 |
Est. completion date | November 2019 |
Est. primary completion date | November 2018 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 50 Years and older |
Eligibility |
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) |
Country | Name | City | State |
---|---|---|---|
Denmark | Odense University Hospital | Odense |
Lead Sponsor | Collaborator |
---|---|
Odense University Hospital | Copenhagen University Hospital, Denmark, Hospital of South West Denmark, Odense Patient Data Explorative Network, Region of Southern Denmark, Sygehus Lillebaelt, University of Southern Denmark |
Denmark,
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* Note: There are 41 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 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) | 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 | Changes in the Bone microarchitecture at the tibia | HRpQCT assesses parameters of bone microarchitecture at the tibia. | 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 | |
Secondary | Changes in the Bone microarchitecture at the radius | HRpQCT assesses parameters of bone microarchitecture at the radius. | 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 | |
Secondary | changes in muscle mass | Full body DXA | at the time the participants start treatment and in an interval as close as possible to after 12 and 24 months from baseline | |
Secondary | Changes from baseline in the markers of bone resorption | CTX, sclerostin | 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 | |
Secondary | Changes from baseline in the markers of bone formation | P1NP | 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 | |
Secondary | Changes in Muscle strength | Measurements of muscle strength (leg extensor power) | 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 | |
Secondary | Changes in handgrip strength | Measurements of muscle strength (handgrip strength) | 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 | |
Secondary | Changes in Balance | Short Physical Performance Battery (SPPB) | 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 | |
Secondary | Adherence to WBV | Self Reporting training log | During 2 years from the start of the treatment | |
Secondary | Changes in physical activity | IPAQ short version | at the time the participants start treatment and in an interval as close as possible to after 12, and 24 months from baseline | |
Secondary | Changes in quality of life | EQ5D questionaire. | at the time the participants start treatment and in an interval as close as possible to after 12, and 24 months from baseline | |
Secondary | Changes in basic mobility | Time up and go test | 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 | |
Secondary | Changes in The Falls Efficacy Scale International | FES-I | at the time the participants start treatment and in an interval as close as possible to after 12, and 24 months from baseline |
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