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Ibuprofen Supplementation After Resistance Training and Its Effects on Bone in Older Women

Primary Purpose

Sarcopenia, Osteoporosis

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Non-steroidal anti-inflammatory drug (Ibuprofen)
placebo
Resistance exercise
Flexibility training
Sponsored by
University of Saskatchewan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Sarcopenia focused on measuring elderly, women, exercise, pQCT, ibuprofen

Eligibility Criteria

65 Years - undefined (Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • women >65yrs

Exclusion Criteria:

  • high risk of fracture
  • use of bisphosphonates, hormone replacement therapy, selective estrogen receptor modulators, PTH, or calcitonin within the past 12 months
  • taking medications that affect bone mineral metabolism
  • have diseases that are known to affect bone mineral metabolism
  • have severe osteoarthritis
  • currently a smoker
  • currently participating in moderate-vigorous resistance-exercise training more than once per week

Sites / Locations

  • College of Kinesiology

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Placebo Comparator

Experimental

Sham Comparator

Arm Label

Non-steroidal anti-inflammatory drug

placebo

resistance exercise

flexibility training

Arm Description

ibuprofen after exercise training sessions (400 mg, 3 times per week for 9 months)

placebo after exercise training sessions(3 times per week for 9 months)

3 sets of 8-12 repetitions of resistance exercises focused on distal radius to be performed 3 times/week for 9 months

flexibility training to be performed 3 days/week for 1 hour for 9 months

Outcomes

Primary Outcome Measures

change from baseline in aBMD of the proximal femur and lumbar spine at 9 months
areal bone mineral density of the proximal femure and lumbar spine assessed by dual energy x-ray absorptiometry

Secondary Outcome Measures

change from baseline in femoral neck section modulus at 9 months
femoral neck section modulus assessed by dual energy x-ray absorptiometry
change from baseline in distal radius Bone Strength Index at 9 months
distal radius Bone Strength Index assessed by high resolution peripheral quantitative computed tomography
change from baseline in radial shaft Stress Strain Index at 9 months
radial shaft Stress Strain Index assessed by peripheral quantitative computed tomography
change from baseline in radial shaft muscle cross-sectional area at 9 months
radial shaft muscle cross-sectional area assessed by peripheral quantitative computed tomography
change from baseline in total body lean tissue mass at 9 months
total body lean tissue mass assessed by dual energy x-ray absorptiometry
change from baseline in muscular strength at 9 months
muscular strength assessed by 1 repetition maximum bicep curl and leg press
change from baseline in balance performance at 9 months
balance performance assessed by tandem walk on balance board

Full Information

First Posted
June 20, 2013
Last Updated
May 2, 2017
Sponsor
University of Saskatchewan
Collaborators
Canadian Institutes of Health Research (CIHR)
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1. Study Identification

Unique Protocol Identification Number
NCT01886196
Brief Title
Ibuprofen Supplementation After Resistance Training and Its Effects on Bone in Older Women
Official Title
Ibuprofen Supplementation After Resistance Training and Its Effects on Bone in Older Women
Study Type
Interventional

2. Study Status

Record Verification Date
May 2017
Overall Recruitment Status
Completed
Study Start Date
April 2013 (undefined)
Primary Completion Date
July 2014 (Actual)
Study Completion Date
July 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Saskatchewan
Collaborators
Canadian Institutes of Health Research (CIHR)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Inflammation increases with aging and is implicated in the reduction of bone mass, muscle mass, and strength. Resistance training is safe and effective for increasing muscle mass and strength in older adults,however resistance training by itself cannot suppress inflammation. Ibuprofen is a non-steroidal anti-inflammatory drug that may provide benefits to muscle mass and strength when given after resistance training sessions in older adults; however, more evidence is required to confirm effects across the lifespan. The objectives are to determine the effect of 9 months of exercise training and ibuprofen supplementation, compared to placebo, in older women (≥65years)on the following dependent variables: bone density, geometry, and architecture muscle mass and strength balance
Detailed Description
The aim of our study is to create new evidence about the effectiveness and safety of non-steroid anti-inflammatory supplementation (i.e. ibuprofen) combined with exercise to influence positively bone and muscle health in women aged 65 years and older. With aging, there is a significant decrease in bone mineral, muscle mass, and strength, which increases the risk of falls, injuries and fracture especially for women. Direct and indirect health costs associated with osteoporosis and sarcopenia (defined as "muscle wasting") are in the billions of dollars and escalating as the proportion of older adults in Canada grows. Low-grade inflammation is a main contributing factor to bone and muscle deterioration with aging but is mitigated by anti-inflammatory drug use. Recent evidence shows resistance exercise training combined with a non-steroidal anti-inflammatory drug (ibuprofen) is effective for increasing bone mineral density in young women. No study has addressed directly the effects of ibuprofen use following resistance exercise on bone and muscle in older women, the population at greatest risk of developing osteoporosis. The primary purpose of this study is to investigate the safety and multiple effects of ibuprofen ingestion following supervised resistance exercise training on bone and muscle in older women (≥65y). PRIMARY HYPOTHESES: Ibuprofen combined with resistance training will maintain hip and lumbar spine areal bone mineral density in older women. Secondary hypotheses are that bone structural properties in the hip and wrist, and muscle mass and strength will be improved by supplementing ibuprofen after resistance training sessions. RESEARCH PLAN: The study will use a repeated measures, parallel group randomized design where 100 women (≥65 y) will be randomized to one of 4 groups: 1) Exercise and ibuprofen (400 mg immediately after exercise); 2) Exercise and ibuprofen placebo; 3) Placebo exercise and ibuprofen, 4) Placebo exercise and ibuprofen placebo. Women will participate in the exercise sessions 3 days per week. The intervention will be 9 months in duration. Dual energy X-ray absorptiometry (DXA) will be used to assess hip and lumbar spine areal bone mineral density, as well as geometric changes in hip structure, and whole body lean tissue (i.e. muscle) mass. Peripheral quantitative computed tomography (pQCT) and high-resolution-pQCT will allow us to investigate detailed changes in bone microarchitecture at the wrist and muscle cross-sectional area in the forearm in response to the intervention. Safety will be addressed by closely monitoring adverse events. RELEVANCE: This pilot study potentially drives a novel post-market use of ibuprofen. In addition, it permits our developing research team a foray into preliminary data collection to inform a larger randomized controlled trial (RCT) application to CIHR.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sarcopenia, Osteoporosis
Keywords
elderly, women, exercise, pQCT, ibuprofen

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Non-steroidal anti-inflammatory drug
Arm Type
Experimental
Arm Description
ibuprofen after exercise training sessions (400 mg, 3 times per week for 9 months)
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
placebo after exercise training sessions(3 times per week for 9 months)
Arm Title
resistance exercise
Arm Type
Experimental
Arm Description
3 sets of 8-12 repetitions of resistance exercises focused on distal radius to be performed 3 times/week for 9 months
Arm Title
flexibility training
Arm Type
Sham Comparator
Arm Description
flexibility training to be performed 3 days/week for 1 hour for 9 months
Intervention Type
Drug
Intervention Name(s)
Non-steroidal anti-inflammatory drug (Ibuprofen)
Other Intervention Name(s)
Ibuprofen
Intervention Description
400mg of ibuprofen administered after exercise training session 3 days per week
Intervention Type
Other
Intervention Name(s)
placebo
Intervention Description
placebo designed to mimic experimental drug (ibuprofen)
Intervention Type
Behavioral
Intervention Name(s)
Resistance exercise
Intervention Description
3 sets of 8-12 repetitions of resistance exercise (full body with a focus on the distal radius) completed 3 days/week under supervision in the research gym
Intervention Type
Behavioral
Intervention Name(s)
Flexibility training
Intervention Description
3 days of full body stretching program (approximately 1 hour) to be performed at participants home unsupervised
Primary Outcome Measure Information:
Title
change from baseline in aBMD of the proximal femur and lumbar spine at 9 months
Description
areal bone mineral density of the proximal femure and lumbar spine assessed by dual energy x-ray absorptiometry
Time Frame
baseline and 9 months
Secondary Outcome Measure Information:
Title
change from baseline in femoral neck section modulus at 9 months
Description
femoral neck section modulus assessed by dual energy x-ray absorptiometry
Time Frame
baseline and 9 months
Title
change from baseline in distal radius Bone Strength Index at 9 months
Description
distal radius Bone Strength Index assessed by high resolution peripheral quantitative computed tomography
Time Frame
baseline and 9 months
Title
change from baseline in radial shaft Stress Strain Index at 9 months
Description
radial shaft Stress Strain Index assessed by peripheral quantitative computed tomography
Time Frame
baseline and 9 months
Title
change from baseline in radial shaft muscle cross-sectional area at 9 months
Description
radial shaft muscle cross-sectional area assessed by peripheral quantitative computed tomography
Time Frame
baseline and 9 months
Title
change from baseline in total body lean tissue mass at 9 months
Description
total body lean tissue mass assessed by dual energy x-ray absorptiometry
Time Frame
baseline and 9 months
Title
change from baseline in muscular strength at 9 months
Description
muscular strength assessed by 1 repetition maximum bicep curl and leg press
Time Frame
baseline and 9 months
Title
change from baseline in balance performance at 9 months
Description
balance performance assessed by tandem walk on balance board
Time Frame
baseline and 9 months
Other Pre-specified Outcome Measures:
Title
number of participants with adverse events as a measure of safety and number of participants wit adverse events as a measure of safety and tolerability
Description
adverse events as reported by participants and charted on 'adverse events' form
Time Frame
continuously throughout 9 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: women >65yrs Exclusion Criteria: high risk of fracture use of bisphosphonates, hormone replacement therapy, selective estrogen receptor modulators, PTH, or calcitonin within the past 12 months taking medications that affect bone mineral metabolism have diseases that are known to affect bone mineral metabolism have severe osteoarthritis currently a smoker currently participating in moderate-vigorous resistance-exercise training more than once per week
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Philip D Chilibeck, PhD
Organizational Affiliation
University of Saskatchewan
Official's Role
Principal Investigator
Facility Information:
Facility Name
College of Kinesiology
City
Saskatoon
State/Province
Saskatchewan
ZIP/Postal Code
S7N5B2
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
18461099
Citation
Krentz JR, Quest B, Farthing JP, Quest DW, Chilibeck PD. The effects of ibuprofen on muscle hypertrophy, strength, and soreness during resistance training. Appl Physiol Nutr Metab. 2008 Jun;33(3):470-5. doi: 10.1139/H08-019.
Results Reference
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Ibuprofen Supplementation After Resistance Training and Its Effects on Bone in Older Women

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