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Mode of Exercise and Bone Biomarkers in Older Veterans (MOVE)

Primary Purpose

Aging, Musculoskeletal Diseases, Osteoporosis

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
10 Weeks of Supervised Resistance Exercise Training
10 Weeks of Supervised Endurance Exercise Training
Sponsored by
VA Office of Research and Development
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Aging

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Healthy older (60+ y) Veteran women and men in the Denver Metro Area
  • Normally active (e.g., recreational cycling or walking exercise)

Exclusion Criteria:

  • Impaired renal function, defined as an eGRF of <60 mL/min/1.73m2
  • Hepatobiliary disease, defined as liver function tests (AST, ALT) >1.5 times the upper limit of normal
  • Thyroid dysfunction, defined as an ultrasensitive thyroid stimulating hormone (TSH) <0.5 or >5.0 mU/L
  • Serum Ca <8.5 or >10.3 mg/dL
  • Serum 25(OH)D <20 ng/mL
  • Uncontrolled hypertension, defined as resting systolic blood pressure (BP) >150 mmHg or diastolic BP >90 mmHg;
  • History of type 1 or type 2 diabetes
  • Cardiovascular disease, defined as subjective or objective indicators of ischemic heart disease (e.g., angina, ST segment depression) or serious arrhythmias at rest or during the graded exercise test (GXT). Volunteers who have a positive GXT can be re-considered after follow-up evaluation, which must include diagnostic testing (e.g., stress echocardiogram or thallium stress test) with interpretation by a cardiologist
  • Anemia, defined as a serum hemoglobin <12.1 g/dL for women and <14.3 g/dL for men
  • Fracture in the past 6 months
  • Current diagnosis or symptoms of COVID-19

In the event of abnormal BP, live function, TSH, 25(OH)D, or hemoglobin values, volunteers can be reassessed, including after appropriate follow-up evaluation and treatment by a primary care provider. Those who have experienced symptoms of COVID-19 or have been formally diagnosed will be allowed to participate once symptoms have resolved and they are approved to return to exercise by their primary care provider.

Sites / Locations

  • Rocky Mountain Regional VA Medical Center, Aurora, CORecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Resistance Exercise

Endurance Exercise

Arm Description

Participants will perform total body resistance training 3x per week for 10 weeks. Each exercise session will last approximately 1 hour.

Participants will complete 60 minutes of stationary cycling 3x per week at 70-80% of maximal heart rate for 10 weeks.

Outcomes

Primary Outcome Measures

c-telopeptide of type 1 collagen (CTX) change
CTX is a marker of bone resorption. Reference range is 0.1-0.8 ng/mL with lower concentrations suggesting less bone resorption
Procollagen 1 intact N-terminal propeptide (P1NP)
PINP is a blood marker of bone formation. Reference range is 19-80 ng/mL with lower concentrations suggesting less bone formation.
Short Physical Performance Battery (SPPB)
The Short Physical Performance Battery will be performed at the beginning and the end of the intervention to assess physical function. Scores range from 0 to 12. Higher scores generally indicate better physical function.
6-minute walk test
The 6-minute walk test will be performed at the beginning and the end of the intervention to assess physical function and fitness. Greater distances covered during the 6 minute walk test generally represent greater function and fitness.

Secondary Outcome Measures

Parathyroid Hormone (PTH)
Parathyroid hormone is a blood marker of parathyroid function. Parathyroid hormone helps to regulate blood calcium levels. The reference range is 14 to 65 pg/mL, with levels in range suggesting normal parathyroid function.
Ionized calcium (iCa)
iCa is measured to understand the stimulus for parathyroid hormone secretion during exercise and to describe patterns of change between modes of exercise.
Total calcium (tCa)
tCa is measured to determine any effects of calcium binding on iCa concentration and to describe patterns of change in tCa between modes of exercise.

Full Information

First Posted
February 9, 2022
Last Updated
July 6, 2023
Sponsor
VA Office of Research and Development
Collaborators
University of Colorado, Denver
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1. Study Identification

Unique Protocol Identification Number
NCT05266976
Brief Title
Mode of Exercise and Bone Biomarkers in Older Veterans
Acronym
MOVE
Official Title
Anabolic Versus Catabolic Skeletal Effects of Endurance or Resistance Exercise in Older Veterans
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 6, 2022 (Actual)
Primary Completion Date
December 1, 2026 (Anticipated)
Study Completion Date
March 31, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development
Collaborators
University of Colorado, Denver

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Adults are often encouraged to exercise to maintain or improve bone health. However, there is evidence that exercise does not always lead to increases in bone mass, and exercise could lead to bone loss under certain conditions. Endurance exercise can increase bone resorption following an exercise bout, which may explain why bone does not always favorably adapt to exercise, but it is unclear if this also happens with resistance exercise. Further, it is not known how exercise training influences blood markers of bone resorption for either endurance or resistance exercise. The purpose of this study is to determine 1) if resistance exercise causes a similar increase in bone resorption as endurance exercise; and 2) if exercise training influences the increase in bone resorption following exercise for both endurance and resistance exercise.
Detailed Description
Exercise is frequently recommended to reduce the risk of osteoporotic fracture. However, bone does not always result in the expected improvements in bone mass, and there is evidence that endurance exercise may lead to bone loss under certain conditions. It is the contention that disruptions in calcium homeostasis during exercise, resulting in a decrease in serum ionized calcium (iCa) and increases in parathyroid hormone (PTH) and c-telopeptide of type I collagen (CTX; a marker of bone resorption) that occur shortly after the start of exercise, may be responsible for the lack of the expected improvements in bone mineral density. The iCa, PTH, and CTX responses to exercise have been well-characterized for both young and older adults in response to a single endurance exercise bout, but it is unclear if resistance training (e.g., weightlifting) results in the same exercise-induced disruption in calcium homeostasis. Further, it is unclear how the iCa, PTH, and CTX response to exercise may change with exercise training, and if a bone anabolic response to exercise can be detected after repeat exercise bouts. The bone anabolic response to exercise (assessed by procollagen of type I terminal propeptide, P1NP; a marker of bone formation) has yet to be fully characterized, but that may be due to the testing of single exercise bouts and the short sampling timeline following exercise. To address these gaps in knowledge, up to 60 Veterans (30 men, 30 women), aged 60-80 years, will be randomized to 1) stationary cycling; or 2) resistance training and will complete 10 weeks of supervised exercise training 3x/week (30 total exercise training sessions). This number of exercise visits was due to the demonstrated increase in P1NP after 28 doses of teriparatide, a PTH analog, that results in bone formation. During the 1st, 15th, and 30th exercise training session, participants will undergo an acute exercise testing bout with pre- and post-exercise sampling up to 48 hours after exercise. Blood samples will be collected to measure iCa, PTH, CTX and P1NP. The primary aims are 1) to determine if resistance exercise results in a different bone biomarker response compared to what the investigators have observed during endurance exercise in older adults; 2) determine if resistance and/or endurance exercise result in an increase in P1NP over 10 weeks of exercise training. Exploratory outcomes related to changes in fitness and functional status will address how Veteran health is impacted by each exercise type, which will be used to inform future applications. The biomarker and functional outcomes information are the next step in determining the appropriate "dose" of exercise, consisting of factors such as exercise type, frequency, duration, and intensity (which will be explored in future research), can be used to enhance Veteran health. Exercise should continue to be recommended for overall health, but future interventions could incorporate what is known about the dose of exercise that is needed for cardiometabolic health and the emerging data on the dose of exercise needed to preserve bone health to create personalized exercise prescriptions to improve multiple components of Veteran health. The proposed research is significant because it is investigating several knowledge gaps that need to be addressed to design future, larger exercise and lifestyle interventions aimed at preserving multiple components of Veteran health, which could have a lasting impact on Veteran quality of life and functional independence. The proposed research is innovative because it is testing novel hypotheses, the mode of exercise on the disruption in calcium homeostasis and the role of exercise training, in a population that could greatly benefit from the knowledge to be gained. Long-term, information gleaned from this research will help to define personalized exercise prescriptions to improve cardiometabolic health without compromising bone health in aging Veterans.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Aging, Musculoskeletal Diseases, Osteoporosis

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Parallel Design with 2 study arms: endurance exercise and resistance exercise
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Resistance Exercise
Arm Type
Experimental
Arm Description
Participants will perform total body resistance training 3x per week for 10 weeks. Each exercise session will last approximately 1 hour.
Arm Title
Endurance Exercise
Arm Type
Experimental
Arm Description
Participants will complete 60 minutes of stationary cycling 3x per week at 70-80% of maximal heart rate for 10 weeks.
Intervention Type
Behavioral
Intervention Name(s)
10 Weeks of Supervised Resistance Exercise Training
Intervention Description
Participants will be randomized to complete 10 weeks of either resistance (weight lifting, hopping) supervised exercise. Exercise will be 3x per week for 1 hour each session. There are a total of 30 exercise sessions.
Intervention Type
Behavioral
Intervention Name(s)
10 Weeks of Supervised Endurance Exercise Training
Intervention Description
Participants will be randomized to complete 10 weeks of endurance (stationary cycling) supervised exercise. Exercise will be 3x per week for 1 hour each session. There are a total of 30 exercise sessions.
Primary Outcome Measure Information:
Title
c-telopeptide of type 1 collagen (CTX) change
Description
CTX is a marker of bone resorption. Reference range is 0.1-0.8 ng/mL with lower concentrations suggesting less bone resorption
Time Frame
Before exercise to up to 48 hours after each exercise bout
Title
Procollagen 1 intact N-terminal propeptide (P1NP)
Description
PINP is a blood marker of bone formation. Reference range is 19-80 ng/mL with lower concentrations suggesting less bone formation.
Time Frame
The primary outcome for Specific Aim 2 is the change in pre-exercise P1NP from the 1st to the 3rd exercise test (approximately 10 weeks apart).
Title
Short Physical Performance Battery (SPPB)
Description
The Short Physical Performance Battery will be performed at the beginning and the end of the intervention to assess physical function. Scores range from 0 to 12. Higher scores generally indicate better physical function.
Time Frame
Change in Short Physical Performance Battery score from the beginning to the end of the 10 week exercise intervention.
Title
6-minute walk test
Description
The 6-minute walk test will be performed at the beginning and the end of the intervention to assess physical function and fitness. Greater distances covered during the 6 minute walk test generally represent greater function and fitness.
Time Frame
Change in the distance covered in the 6-minute walk test from the beginning to the end of the10 week exercise intervention.
Secondary Outcome Measure Information:
Title
Parathyroid Hormone (PTH)
Description
Parathyroid hormone is a blood marker of parathyroid function. Parathyroid hormone helps to regulate blood calcium levels. The reference range is 14 to 65 pg/mL, with levels in range suggesting normal parathyroid function.
Time Frame
The change in serum PTH from before exercise to the peak following exercise following each exercise test. Peak could occur up to 48 hours following exercise.
Title
Ionized calcium (iCa)
Description
iCa is measured to understand the stimulus for parathyroid hormone secretion during exercise and to describe patterns of change between modes of exercise.
Time Frame
Serum iCa is measured before exercise (-15, 0 minutes) and after exercise (60, 120, 300 minutes and 24 and 48 hours),
Title
Total calcium (tCa)
Description
tCa is measured to determine any effects of calcium binding on iCa concentration and to describe patterns of change in tCa between modes of exercise.
Time Frame
Serum tCa is measured before exercise (-15, 0 minutes) and after exercise (60, 120, 300 minutes and 24 and 48 hours).
Other Pre-specified Outcome Measures:
Title
VO2peak from graded exercise test (GXT)
Description
A cycling GXT will be performed at the beginning and the end of the exercise intervention to measure aerobic fitness. Higher values represent greater aerobic fitness.
Time Frame
Change in VO2 peak from the beginning to the end of the 10 week exercise intervention.
Title
1-repetition maximum (1RM)
Description
1RM of leg press will be measured at the beginning and the end of the 10 week exercise intervention to measure muscle strength. Higher weights performed during the test indicated greater muscle strength.
Time Frame
Change in leg press 1RM from the beginning to the end of the 10 week exercise intervention.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy older (60+ y) Veteran women and men in the Denver Metro Area Normally active (e.g., recreational cycling or walking exercise) Exclusion Criteria: Impaired renal function, defined as an eGRF of <60 mL/min/1.73m2 Hepatobiliary disease, defined as liver function tests (AST, ALT) >1.5 times the upper limit of normal Thyroid dysfunction, defined as an ultrasensitive thyroid stimulating hormone (TSH) <0.5 or >5.0 mU/L Serum Ca <8.5 or >10.3 mg/dL Serum 25(OH)D <20 ng/mL Uncontrolled hypertension, defined as resting systolic blood pressure (BP) >150 mmHg or diastolic BP >90 mmHg; History of type 1 or type 2 diabetes Cardiovascular disease, defined as subjective or objective indicators of ischemic heart disease (e.g., angina, ST segment depression) or serious arrhythmias at rest or during the graded exercise test (GXT). Volunteers who have a positive GXT can be re-considered after follow-up evaluation, which must include diagnostic testing (e.g., stress echocardiogram or thallium stress test) with interpretation by a cardiologist Anemia, defined as a serum hemoglobin <12.1 g/dL for women and <14.3 g/dL for men Fracture in the past 6 months Current diagnosis or symptoms of COVID-19 In the event of abnormal BP, live function, TSH, 25(OH)D, or hemoglobin values, volunteers can be reassessed, including after appropriate follow-up evaluation and treatment by a primary care provider. Those who have experienced symptoms of COVID-19 or have been formally diagnosed will be allowed to participate once symptoms have resolved and they are approved to return to exercise by their primary care provider.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sarah J Wherry, PhD
Phone
(720) 848-6475
Email
sarah.wherry@va.gov
First Name & Middle Initial & Last Name or Official Title & Degree
Toby Wellington, MS
Phone
(720) 848-6376
Email
toby.wellington@va.gov
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sarah J Wherry, PhD
Organizational Affiliation
Rocky Mountain Regional VA Medical Center, Aurora, CO
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rocky Mountain Regional VA Medical Center, Aurora, CO
City
Aurora
State/Province
Colorado
ZIP/Postal Code
80045
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Todd R Furbacher, PhD
Phone
720-857-5105
Email
todd.furbacher@va.gov
First Name & Middle Initial & Last Name & Degree
Kimberly K Owens, MPH
Phone
(720) 857-5667
Email
kimberly.owens9@va.gov
First Name & Middle Initial & Last Name & Degree
Sarah J Wherry, PhD

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Because some journals now require authors to provide access to data, de-identified and anonymized data sets including both individual- and group-level data will be created after publication of manuscripts. The data will be made available upon request for general research purposes. To the extent possible, all care will be taken to ensure that individual-level data are at very low risk for re-identification and there will be no links to personally identifiable information.
IPD Sharing Time Frame
There is no formal plan to share these documents, although requests will be considered. Information describing the protocol and statistical analysis plan will be in place when study results are published.
IPD Sharing Access Criteria
Data will become available after publication of study results and will be available for at least 3 years beyond the completion of the study.

Learn more about this trial

Mode of Exercise and Bone Biomarkers in Older Veterans

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