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OsteoVelocity - Effects of different Velocities in Resistance Training on Bone Mineral Density in Women: A Randomized Controlled Trial

OsteoVelocity - Effects of different Velocities in Progressive Resistance Training on Bone Mineral Density in Healthy Women over 45: A Pilot of a Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12624001276549
Enrollment
51
Registered
2024-10-18
Start date
2025-03-19
Completion date
2025-06-08
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Bone loss is a common health problem in older people, particularly women, and can significantly affect their quality of life. Progressive resistance training has been shown to be effective in preventing bone loss. However, several questions remain regarding the optimal design of such interventions. One such aspect is movement velocity. The aim of this project is to investigate whether faster movement velocities are more effective in improving bone mineral density.

Interventions

Participants in the intervention groups 'high strain training' (HST) and 'low strain training' (LST) will participate in two supervised resistance training sessions per week for a duration of 6 months. Each session will last approximately 1 hour and 15 minutes. Training will be conducted in small groups with a maximum of 7 participants per group. A researcher will explain the exercises and all relevant parameters (e.g., movement velocity, range of motion, rest period, etc.) to the participants.

Participants in the intervention groups 'high strain training' (HST) and 'low strain training' (LST) will participate in two supervised resistance training sessions per week for a duration of 6 months. Each session will last approximately 1 hour and 15 minutes. Training will be conducted in small groups with a maximum of 7 participants per group. A researcher will explain the exercises and all relevant parameters (e.g., movement velocity, range of motion, rest period, etc.) to the participants. Furthermore, a researcher will observe and provide corrective feedback to the participants during their performance. The feedback will encompass aspects such as posture, breathing, range of motion, tempo, and muscle engagement. Every mesocycle will begin with a two-week period of low-intensity exercise for learning purposes, followed by a five-week phase of moderate intensity and another five weeks of high-intensity training. The Borg Rating of Percieved Exertion Scale (RPE) and repetition ranges will be used to guide exercise intensity. Moderate intensity, approximately 65-75% of one repetition maximum (1 RM), will involve 10 to 15 repetitions, while high intensity, about 80-90% of 1 RM, will consist of 8 to 5 repetitions. The achieved weight and RPE will be recorded in the training log book for each exercise and set. Subsequently, the exercises will be modified. While the initial half of the intervention primarily incorporates less complex exercises on machines (e.g., leg press), the latter half will introduce more intricate movements (e.g., squats). Prior to each progressive resistance training session, there will be a general warm-up and a brief specific warm-up with drills to acclimate participants to the anticipated movement velocity. The intervention groups differ solely in the targeted movement velocity. The HST group will execute all exercises with an explosive concentric phase, a brief isometric hold at the turning point, and an eccentric phase at moderate velocity (X/1/2). The LST group will perform all exercises with an explosive concentric phase, a brief isometric hold at the turning point, and an extended eccentric phase (X/1/4). Both active groups will be instructed to execute the concentric phase at maximal velocity (X). The HST group will be directed to perform the eccentric phase at moderate velocity (2s), while the LST group will be instructed to execute a slow eccentric phase (4s). Session attendance will be recorded in the training logbook.

Sponsors

University of Adelaide
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
45 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Healthy untrained women over 45

Exclusion criteria

• Not fluent in English • Current smokers • Pregnancy • Breastfeeding • Trained (Participated in resistance training or a structured weight-bearing exercise program at least once a week in the past 12 months) • Inability to participate in a supervised exercise program if assigned. • Contraindications to participating in vigorous physical activity • Cardiovascular disease • Cognitive impairment • Recent radiotherapy • Joint injury or surgery • Fracture (within the past 12 months) • Depression • Medications known to affect bone • Medical conditions known to affect bone health • Osteoporosis (T-Score under -2,5) • Obesity (BMI > 30) • High alcohol consumption (more than 14 standard drinks per week)

Outcome results

None listed

Source: ANZCTR · Data processed: Apr 4, 2026