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An examination of Calf Raise Test protocol variations in healthy adults

Effect of Calf Raise Test protocol variations in healthy participants: A randomised cross-over study

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12625001325493
Enrollment
35
Registered
2025-11-28
Start date
2026-03-30
Completion date
2026-06-05
Last updated
2025-12-08

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

Conditions

None listed

Brief summary

This project aims to explore the potential effect of variations on calf raise test protocol on outcomes, namely that of cadence (self select, 60 bpm, and as fast as possible), footwear (barefoot vs footwear), and target height (with vs without overhead height). These variations are all used in research and practice, and would be informative to researchers and clinicians.

Interventions

This is a randomised cross-over study performed in a biomechanics laboratory in three parts to examine the effects of (1) cadence; (2) target height; and (3) footwear on outcomes. Participants will complete the calf raise test to fatigue following established protocols from Hebert-Losier et al. Participants will be asked to go up and down on their toes as many times as possible, standing on one leg on a 10 degrees incline following the beat of a metronome. To assist balance, individuals will

This is a randomised cross-over study performed in a biomechanics laboratory in three parts to examine the effects of (1) cadence; (2) target height; and (3) footwear on outcomes. Participants will complete the calf raise test to fatigue following established protocols from Hebert-Losier et al. Participants will be asked to go up and down on their toes as many times as possible, standing on one leg on a 10 degrees incline following the beat of a metronome. To assist balance, individuals will be permitted to apply fingertip support at shoulder height on a wall in front of them. Participants will be instructed to lift the heel as high as possible for each calf raise, keeping the knee and trunk straight. A trained physiotherapist, strength & conditioning coach, or sport scientist with human movement expertise will supervise adherence to the test protocol. Participants will only complete one condition in one session. Therefore, participants will be asked to attend repeat sessions 7 to 14 days apart and perform the test in one condition, allocated in a randomised order, until all conditions are completed. Accordingly, the minimum washout period will be 7 days between conditions, and the maximum will be 14 days. A participant will therefore be involved in the study for a period of 2 to 4 weeks in total. Note that different cohorts of participants will be recruited to examine the effects of (1) cadence; (2) target height; and (3) footwear. Variation 1 (cadence): 1.a 60 bpm barefoot without an overhead target; 1.b self-selected cadence barefoot without an overhead target; 1.c as fast as possible cadence barefoot without an overhead target. Note that a pilot trial will be conducted where individuals only complete 10 repetitions, and attend one single session only with 20 minutes rest between conditions. This pilot trial is part of this registration. The number of participant is the same, with the purpose of testing participants in a non-fatigue state with relevance to training and rehabilitation. This pilot will take place before the fatigue experimentation, and analysed alongside the fatigue trial. Variation 2 (target height): 2a. 60 bpm, barefoot, without an overhead target; 2b. 60 bpm, barefoot, with an overhead target. Variation 3 (footwear): 3a. 60 bpm, barefoot, without an overhead target; 3b. 60 bpm, standardised footwear (Aero Glide 2), without an overhead target.

Sponsors

Kim Hebert-Losier - University of Waikato
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Diagnosis
Masking
Open (masking not used)

Eligibility

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

Inclusion criteria

Free of injury, illness, or conditions that may affect movements or landing mechanics. Free of lower extremity, back, or pelvis injury in the last three months. No history of Achilles tendon rupture.

Exclusion criteria

None

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026