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The Effect of High Impact Exercise on Bone and Articular Cartilage in Post-menopausal Women

Primary Purpose

Osteoporosis, Postmenopausal, Osteoarthritis, Knee, BMD

Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Hopping
Sponsored by
Loughborough University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Osteoporosis, Postmenopausal focused on measuring Exercise, Osteoporosis, Osteoarthritis, MRI, DXA, High Impact, Cartilage, Bone

Eligibility Criteria

55 Years - 70 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Post-menopausal - at least 12 months since last menstruation and/or hysterectomy, oophorectomy or hormonal contraceptive use

Exclusion Criteria:

  • Existing knee, hip or back injury.
  • Any medical conditions or injuries which exclude participation in an exercise intervention e.g. heart conditions, hypertension
  • BMI > 30 kg/m2
  • Participation in a study involving ionising radiation in the previous 12 months.
  • Exercise involving ground reaction forces greater than that of jogging more than once a week.
  • Contraindications to MRI or DXA
  • Osteoporotic (FRAX score requiring the participant is advised to seek treatment)
  • Medication affecting bone metabolism or density

Sites / Locations

  • Loughborough UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

Exercise Leg

Non exercise Leg

Arm Description

Left or right leg randomly assigned as exercise leg in a unilateral, exercise intervention. This will be a progressive exercise programme with the aim being to complete 50 multidirectional hops completed daily. (Hopping)

Randomly assigned non-exercise, control leg.

Outcomes

Primary Outcome Measures

Change in T2 Relaxation Time (ms)
T2 mapping is an indicator of the water content in cartilage, with longer relaxation times a marker of cartilage degeneration

Secondary Outcome Measures

Change in Femoral neck bone mineral density (g/cm2)
Change in Femoral neck bone mineral content (g)
Change in Spine bone mineral density (g/cm2)
Change in Spine bone mineral content (g)
Change in Postural sway (mm)
Change in Maximal hop height (mm)
Change in Ground Reaction force Maximal Hop (N)
Change in Ground Reaction force for a set of ten hops (N)
Change in BMD(D100) (mg HA/cm3)
Volumetric Bone mineral density
Change in Total bone mass (mg)
Change in BV/TV (%)
Percent bone volume
Change in pBV/TV (%)
Plate bone volume fraction
Change in rBV/TV (%)
Rod bone volume fraction
Change in pBV/rBV (%)
Plate to - rod ratio
Change in pBV/BV (%)
Plate tissue fraction
Change in rBV/BV (%)
Rod tissue fraction
Change in Bone surface(BS) (mm2)
Change in BS/TV (mm-1)
Bone surface density
Change in Tb.Th (mm)
Trabecular thickness
Change in Tb.Sp (mm)
Trabecular Separation
Change in Tb.N (mm-1)
Trabecular number
Change in Tb.Pf
Trabecular bone pattern (Tb.PF) follows the course of stress lines in the bone. This measurement indicates where the bone is under increased stress.
Change in Conn.D (mm-3)
Connectivity density
Change in DA
Degree of anisotropy
Change in τ
Tortuosity (τ) is a measure of how well a structure can curve and bend easily. This is an indicator of where the most stress is on the bone structure.
Change in SMI
Structural model index
Change in BRV (mm3)
Bone resorption volume
Change in BFV (mm3)
Bone formation volume
Change in BRM (mg)
Bone resorption mass
Change in BFM (mg)
Bone formation mass
Change in BRF (%)
Bone resorption fraction
Change in BFF(%)
Bone formation fraction
Change in BRR(mm3/week)
Bone resorption rate
Change in BFR(mm3/week)
Bone formation rate
Change in Trabecular orientation distribution (Tb.O.D) (angle in degrees)
This is a measurement of the orientation of the trabeculae in the distal tibia relative to the central axis tibial shaft. The orientation can be categorised into transvers direction and longitudinal direction along the tibial shaft
Change in Ct.Th(mm)
Cortical thickness
Change in B.Po(%)
Bone porosity
Change in Po.Dm(mm)
Pore diameter
Change in Pore volume distribution
Change in Failure load (N)
Change in Strain
This analyses the change in length of the bone over the time period, expressed as % change.
Change in Stiffness (N/mm)
Change in Young's Modulus (GPa)
Change in Mechanical anisotropic ratio
Change in Strain energy density (J/m3)
Change in Strain gradient (με/mm)

Full Information

First Posted
April 5, 2017
Last Updated
July 18, 2017
Sponsor
Loughborough University
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1. Study Identification

Unique Protocol Identification Number
NCT03225703
Brief Title
The Effect of High Impact Exercise on Bone and Articular Cartilage in Post-menopausal Women
Official Title
The Effect of High Impact Exercise on Bone and Articular Cartilage in Post-menopausal Women
Study Type
Interventional

2. Study Status

Record Verification Date
July 2017
Overall Recruitment Status
Unknown status
Study Start Date
January 2017 (Actual)
Primary Completion Date
June 2018 (Anticipated)
Study Completion Date
January 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Loughborough University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Osteoarthritis (OA) and osteoporosis (OP) affect large numbers of the population. Around 8 million people in the UK are affected by OA and over 300,000 people present with fragility fractures in the UK each year. High impact exercise has been shown to improve markers of bone health but the effect of this exercise on the cartilage is less well understood. A six month, one leg, exercise program based on hopping will be carried out by a group of post-menopausal women. Post-menopausal women are particularly at risk from OP and the research should give information on the feasibility of this type of exercise program in this age group and the effect on cartilage. Participants will be aged between 55 and 70 (at least five years post menopause) with no conditions that would limit their ability to complete the exercise program. To assess changes in participants' cartilage and bone properties they will be asked to attend several meetings at Loughborough University. Before and after the exercise program participants will have bone density scans and MRI scans of the knee joint. A subset (n=4) will undergo high resolution bone scans that can demonstrate changes in bone structure. The intervention is a home based exercise programme lasting approximately 10 minutes per day. Initially this will be individualised to each participant with the end goal being daily exercise sessions. The programme will last for six months with supervised sessions offered throughout the trial. Using an intervention affecting just one leg will allow the research team to use the other leg as a control. The research team hypothesise that in a population of post-menopausal women, a six month, unilateral exercise intervention will improve bone mineral density at the proximal femur with no negative effects on articular cartilage.
Detailed Description
The research is a 6 month, intervention study of unilateral (single limb) exercise with the changes in a randomly chosen exercise leg being compared to those in the other (control) leg. Potential participants (women aged 55-70) will be approached via existing links in the community, at local community centres, through local media, posters and flyers. After initial contact to determine whether they meet the inclusion/exclusion criteria they will be invited to join the study and sent the participant information sheet (PIS). If they then wish to aid in the research they will be invited to a first meeting at Loughborough University. At the initial meeting the participant can further discuss the project and PIS with the research team. If they fully understand the project and are happy to take part they will be invited to sign the informed consent form. At this stage each participant will be anonymised using a project code. Screening and baseline measurements will then be taken. Screening questionnaires will be taken following consent to the study. These include a demographic questionnaire, health screen questionnaire, calcium intake questionnaire, physical activity readiness questionnaire (PAR-Q) and bone physical activity questionnaire (BPAQ). Dual X-ray Absorptiometry (DXA) scans of the whole body, anterior-posterior (AP) spine and dual femur will be taken for each participant to give baseline measurements of bone mineral density.Standard positioning procedures for the measurement being taken will be utilised to allow the calculation of the T-score. Functional tests will be performed to investigate hopping and balance ability. Unilateral balance will be analysed by measuring postural sway using a force platform. Participants will be asked to balance on one leg for up to 30 seconds. Amplitude of displacement will be calculated, this is the distance between the maximum and minimum centre of pressure (COP) in both directions. COP path length is the total distance travelled and will be calculated and divided by the trial time to give the COP velocity. Maximal hop height will be measured by recording the vertical displacement of a marker placed on the lumbar spine of each participant whilst conducting a maximal hop. This will be repeated for each leg. The ground reaction force (GRF) of the maximal hop will be recorded using a force platform. Participants will be asked to remain still on the platform for 5 seconds to determine body weight. From this position participants will be asked to lift one leg from the platform and perform a counter movement, maximal hop using their arms to help with propulsion and ensure maximal hop height. After one or two familiarisation attempts the participant will be asked to complete three maximal hops. Allowing for repeats if they do not land fully on the force platform. The peak GRF recorded from these three attempts will be used in the final analysis. Ground reaction forces during a set of ten hops, which is the end goal of the exercise programme, will be recorded on a force platform. Participants will be asked to remain still on the platform for 5 seconds to determine body weight. From this position participants will be asked to lift one leg from the platform and perform ten counter movement hops using their arms to help with propulsion if able. At the baseline measurements participants will be asked to perform ten hops to the best of their ability, with a rigid support available for them to lean on A second appointment will be arranged to acquire baseline MRI scans of each knee joint. This will involve the safety checks, conversation with the radiographers and scan times of up to one hour. Following the MRI scans the exercise leg will be randomly assigned using opaque envelopes. Each envelope will contain a note saying either 'left leg' or 'right leg'. The envelopes will be split into smaller subgroups of eight for minimisation. This will remove the possibility of the first half of volunteers choosing the same leg and removing the randomisation effect on the second half. Participants will be presented with a training diary and instructions on how to complete the exercise programme over six months. The first day of exercise will be completed with the research team at this appointment and the intervention considered started. This second meeting should last for approximately 90 minutes. The required exercise lasts for no longer than 10 minutes each session and can be performed at home. The intervention will be personalised to the individual's ability and the frequency of the exercise will steadily increase as the participant improves, until the exercise is completed daily. Regular group sessions at Loughborough University will be offered to all participants. The exercise time will remain at ten minutes but the session will be longer, allowing for discussion and check-ups with participants. These will be weekly sessions for the first two months and then once a month for the remaining time. Follow up measurements will take place six months after the commencement of the exercise programme. Repeat DXA, MRI and functional outcome tests will be carried out on all participants, following the same protocol as at baseline. Again this will occur over two meetings at Loughborough University. A subset (n=4) will undergo high resolution bone scans (HR-pQCT) that can demonstrate changes in bone structure. This measurement will be taken at the distal tibia and lasts around three minutes per leg. Measurements will be taken pre and post the six month exercise intervention. Descriptive statistics will be calculated to give information on mean values and variation (standard deviation) of the cohort. This will include age, height, body mass, BMI and time since last menstruation. Using Levene's test when comparing the exercise to control leg and Mauchly's test of sphericity to compare from baseline to end of study, the variance of the data will be analysed. Normal distribution will be analysed using Shapiro-Wilks test and visual examination of Q-Q plot. If variance is shown to be homogenous and distribution normal within the population then a repeated measures analysis of variance (RM-ANOVA)will be used to detect any significant differences between leg (exercise versus control, time (baseline versus post-intervention) or leg x time interaction in the outcome variable described previously. If any of the outcome measures do not meet the assumptions to conduct parametric tests i.e. ANOVA then Kruskal-Wallis H test will be used to detect any significant change in differences.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoporosis, Postmenopausal, Osteoarthritis, Knee, BMD
Keywords
Exercise, Osteoporosis, Osteoarthritis, MRI, DXA, High Impact, Cartilage, Bone

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants will complete a unilateral exercise intervention and be randomly assigned an exercise leg. This allows for internal control, non exercise leg. The exercise and control leg will be analysed for significant differences following completion of the intervention.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
32 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Exercise Leg
Arm Type
Active Comparator
Arm Description
Left or right leg randomly assigned as exercise leg in a unilateral, exercise intervention. This will be a progressive exercise programme with the aim being to complete 50 multidirectional hops completed daily. (Hopping)
Arm Title
Non exercise Leg
Arm Type
No Intervention
Arm Description
Randomly assigned non-exercise, control leg.
Intervention Type
Behavioral
Intervention Name(s)
Hopping
Intervention Description
A unilateral, hopping based exercise programme lasting six months.
Primary Outcome Measure Information:
Title
Change in T2 Relaxation Time (ms)
Description
T2 mapping is an indicator of the water content in cartilage, with longer relaxation times a marker of cartilage degeneration
Time Frame
6 months (pre and post intervention)
Secondary Outcome Measure Information:
Title
Change in Femoral neck bone mineral density (g/cm2)
Time Frame
6 months (pre and post intervention)
Title
Change in Femoral neck bone mineral content (g)
Time Frame
6 months (pre and post intervention)
Title
Change in Spine bone mineral density (g/cm2)
Time Frame
6 months (pre and post intervention)
Title
Change in Spine bone mineral content (g)
Time Frame
6 months (pre and post intervention)
Title
Change in Postural sway (mm)
Time Frame
6 months (pre and post intervention)
Title
Change in Maximal hop height (mm)
Time Frame
6 months (pre and post intervention)
Title
Change in Ground Reaction force Maximal Hop (N)
Time Frame
6 months (pre and post intervention)
Title
Change in Ground Reaction force for a set of ten hops (N)
Time Frame
6 months (pre and post intervention)
Title
Change in BMD(D100) (mg HA/cm3)
Description
Volumetric Bone mineral density
Time Frame
6 months (pre and post intervention)
Title
Change in Total bone mass (mg)
Time Frame
6 months (pre and post intervention)
Title
Change in BV/TV (%)
Description
Percent bone volume
Time Frame
6 months (pre and post intervention)
Title
Change in pBV/TV (%)
Description
Plate bone volume fraction
Time Frame
6 months (pre and post intervention)
Title
Change in rBV/TV (%)
Description
Rod bone volume fraction
Time Frame
6 months (pre and post intervention)
Title
Change in pBV/rBV (%)
Description
Plate to - rod ratio
Time Frame
6 months (pre and post intervention)
Title
Change in pBV/BV (%)
Description
Plate tissue fraction
Time Frame
6 months (pre and post intervention)
Title
Change in rBV/BV (%)
Description
Rod tissue fraction
Time Frame
6 months (pre and post intervention)
Title
Change in Bone surface(BS) (mm2)
Time Frame
6 months (pre and post intervention)
Title
Change in BS/TV (mm-1)
Description
Bone surface density
Time Frame
6 months (pre and post intervention)
Title
Change in Tb.Th (mm)
Description
Trabecular thickness
Time Frame
6 months (pre and post intervention)
Title
Change in Tb.Sp (mm)
Description
Trabecular Separation
Time Frame
6 months (pre and post intervention)
Title
Change in Tb.N (mm-1)
Description
Trabecular number
Time Frame
6 months (pre and post intervention)
Title
Change in Tb.Pf
Description
Trabecular bone pattern (Tb.PF) follows the course of stress lines in the bone. This measurement indicates where the bone is under increased stress.
Time Frame
6 months (pre and post intervention)
Title
Change in Conn.D (mm-3)
Description
Connectivity density
Time Frame
6 months (pre and post intervention)
Title
Change in DA
Description
Degree of anisotropy
Time Frame
6 months (pre and post intervention)
Title
Change in τ
Description
Tortuosity (τ) is a measure of how well a structure can curve and bend easily. This is an indicator of where the most stress is on the bone structure.
Time Frame
6 months (pre and post intervention)
Title
Change in SMI
Description
Structural model index
Time Frame
6 months (pre and post intervention)
Title
Change in BRV (mm3)
Description
Bone resorption volume
Time Frame
6 months (pre and post intervention)
Title
Change in BFV (mm3)
Description
Bone formation volume
Time Frame
6 months (pre and post intervention)
Title
Change in BRM (mg)
Description
Bone resorption mass
Time Frame
6 months (pre and post intervention)
Title
Change in BFM (mg)
Description
Bone formation mass
Time Frame
6 months (pre and post intervention)
Title
Change in BRF (%)
Description
Bone resorption fraction
Time Frame
6 months (pre and post intervention)
Title
Change in BFF(%)
Description
Bone formation fraction
Time Frame
6 months (pre and post intervention)
Title
Change in BRR(mm3/week)
Description
Bone resorption rate
Time Frame
6 months (pre and post intervention)
Title
Change in BFR(mm3/week)
Description
Bone formation rate
Time Frame
6 months (pre and post intervention)
Title
Change in Trabecular orientation distribution (Tb.O.D) (angle in degrees)
Description
This is a measurement of the orientation of the trabeculae in the distal tibia relative to the central axis tibial shaft. The orientation can be categorised into transvers direction and longitudinal direction along the tibial shaft
Time Frame
6 months (pre and post intervention)
Title
Change in Ct.Th(mm)
Description
Cortical thickness
Time Frame
6 months (pre and post intervention)
Title
Change in B.Po(%)
Description
Bone porosity
Time Frame
6 months (pre and post intervention)
Title
Change in Po.Dm(mm)
Description
Pore diameter
Time Frame
6 months (pre and post intervention)
Title
Change in Pore volume distribution
Time Frame
6 months (pre and post intervention)
Title
Change in Failure load (N)
Time Frame
6 months (pre and post intervention)
Title
Change in Strain
Description
This analyses the change in length of the bone over the time period, expressed as % change.
Time Frame
6 months (pre and post intervention)
Title
Change in Stiffness (N/mm)
Time Frame
6 months (pre and post intervention)
Title
Change in Young's Modulus (GPa)
Time Frame
6 months (pre and post intervention)
Title
Change in Mechanical anisotropic ratio
Time Frame
6 months (pre and post intervention)
Title
Change in Strain energy density (J/m3)
Time Frame
6 months (pre and post intervention)
Title
Change in Strain gradient (με/mm)
Time Frame
6 months (pre and post intervention)

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
55 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Post-menopausal - at least 12 months since last menstruation and/or hysterectomy, oophorectomy or hormonal contraceptive use Exclusion Criteria: Existing knee, hip or back injury. Any medical conditions or injuries which exclude participation in an exercise intervention e.g. heart conditions, hypertension BMI > 30 kg/m2 Participation in a study involving ionising radiation in the previous 12 months. Exercise involving ground reaction forces greater than that of jogging more than once a week. Contraindications to MRI or DXA Osteoporotic (FRAX score requiring the participant is advised to seek treatment) Medication affecting bone metabolism or density
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Christopher M Hartley, MSC
Email
c.hartley@lboro.ac.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Katherine Brooke-Wavell, PhD
Phone
01509 222749
Email
k.s.f.brooke-wavell@lboro.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Katherine Brooke-Wavel, PhD
Organizational Affiliation
Loughborough University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Loughborough University
City
Loughborough
State/Province
Leicestershire
ZIP/Postal Code
LE11 3TU
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Christopher M Hartley, MSc
Email
c.hartley@lboro.ac.uk
First Name & Middle Initial & Last Name & Degree
Katherine Brooke-Wavell, PhD
Phone
01509 222749
Email
k.s.f.brooke-wavell@lboro.ac.uk
First Name & Middle Initial & Last Name & Degree
Chris Hartley, MSc
First Name & Middle Initial & Last Name & Degree
Katherine Brooke-Wavell, PhD
First Name & Middle Initial & Last Name & Degree
Jonathan Folland, PhD
First Name & Middle Initial & Last Name & Degree
Robert Kerslake

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
There is a plan to have scans available on a public database.
Citations:
PubMed Identifier
33196852
Citation
Du J, Hartley C, Brooke-Wavell K, Paggiosi MA, Walsh JS, Li S, Silberschmidt VV. High-impact exercise stimulated localised adaptation of microarchitecture across distal tibia in postmenopausal women. Osteoporos Int. 2021 May;32(5):907-919. doi: 10.1007/s00198-020-05714-4. Epub 2020 Nov 16.
Results Reference
derived

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The Effect of High Impact Exercise on Bone and Articular Cartilage in Post-menopausal Women

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