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Effect of Upper Limb Isometric Training on Hamstring Activation among Healthy Adults

Acute Effect of Upper Limb Isometric Training on Hamstring Activation among Able-Bodied Adults: A Cross-over Experimental Study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12625000113459
Enrollment
15
Registered
2025-01-31
Start date
2025-02-17
Completion date
2025-09-10
Last updated
2026-02-02

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 study aims to evaluate the acute effects of upper limb isometric training (ULIT) on hamstring activation in able-bodied adults using surface electromyography (sEMG). We hypothesise that the ULIT will significantly improve hamstring activation. Fifteen participants will complete two intervention sessions: one involving submaximal ULIT contractions and another with maximal ULIT contractions, separated by a seven-day washout period. Each intervention session includes three isometric exercises targeting upper limb muscles linked to the posterior myofascial chain, potentially influencing the hamstrings. Hamstring activation will be assessed at baseline, during the exercises, and immediately post-intervention using sEMG to capture peak muscle activity. The findings will offer new insights into interlimb muscle coordination and the role of ULIT in influencing lower limb muscle activation.

Interventions

This crossover trial will take place at the Clinical Examination Laboratory of Hospital Canselor Tuanku Muhriz (HCTM) in Malaysia. Participants will be recruited via convenience sampling through advertisements on campus bulletin boards, social media groups, and the university staff email directory. Eligibility will be determined by a health questionnaire that assesses exclusion criteria, footedness, and dominant leg. Participants who meet the inclusion criteria will sign a consent form after rec

This crossover trial will take place at the Clinical Examination Laboratory of Hospital Canselor Tuanku Muhriz (HCTM) in Malaysia. Participants will be recruited via convenience sampling through advertisements on campus bulletin boards, social media groups, and the university staff email directory. Eligibility will be determined by a health questionnaire that assesses exclusion criteria, footedness, and dominant leg. Participants who meet the inclusion criteria will sign a consent form after receiving detailed information about the study. Potential participants will be recruited to complete two sessions of bilateral upper limb isometric training (ULIT): (1) submaximal contraction and (2) maximal contraction. Each session will include three bilateral ULIT exercises performed in a standing position: Exercise 1: Isometric Wall Push-Up, Exercise 2: Isometric Shoulder Extension, and Exercise 3: Isometric Shoulder External Rotation. These exercises aim to target muscle groups across the posterior myofascial kinetic chain, considering possible interconnections with the hamstrings. The Nicolet EDX system will assess changes in hamstring muscle activity using surface electrodes placed across the semitendinosus, biceps femoris, rectus abdominis, and lower trapezius muscles of the dominant limb. Electrodes are positioned parallel to the muscle fibers in accordance with the SENIAM (Surface ElectroMyoGraphy for the Non-Invasive Assessment of Muscles) guidelines. Muscle activation will be measured using the root mean square (RMS) of peak amplitude. To improve interpretability, RMS values are expressed as percentages relative to a baseline and averaged over 5-second isometric contractions. Muscle activity ratios for each exercise are calculated using the following formula: Ratio (%) = (muscle activity during ULIT exercise/muscle activity during two-foot quiet standing) × 100. Familiarisation Session: Prior to the experimental trials, all participants will undergo a familiarisation session at least three days before the first intervention session to familiarise themselves with the ULIT protocol and the equipment used for hamstring activation measurements. During this session, participants will practice the isometric exercises and apply surface electromyography (sEMG) sensors to ensure proper placement and comfort. The final analysis will not utilise any data from the familiarisation session. The familiarisation session will last approximately 30 minutes. Intervention Session: The interventions will be conducted by a physiotherapist with more than five years of clinical experience. Following the attachment of the electrodes, there is a 15-minute interval before the intervention begins. An outcome evaluator, blinded to the intervention sequence and intensity, will assess outcome measurements at three time points: pre-intervention (baseline measurement), during the intervention exercise (primary outcome measure), and post-intervention (secondary outcome measure). Participants' baseline assessment is taken for the hamstring flexibility of the dominant leg, the maximal voluntary isometric contraction (MVIC) of hamstring peak force and muscle activation during two-foot quiet standing (anatomical position stance width). Each intervention exercise series will be conducted in a similar order, starting with a 5-second maximal effort trial for each exercise. Next, the participants will be verbally ordered to exert either 50% (submaximal ULIT session) or 100% (maximal contraction ULIT session) of their maximum effort, maintaining it for 5 seconds, followed by 5 seconds of rest between each repetition, for a total of 5 repetitions. To minimise muscular fatigue, a one-minute break is given between each exercise. During ULIT exercises, participants will have a hand-held dynamometer attached to their distal hand to monitor force production and ensure consistent effort. An additional effort will be performed if any measured strength exceeds or is less than 10% of the target. The total intervention session will last approximately 60 minutes.

Sponsors

Hospital Canselor Tuanku Muhriz UKM
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Treatment
Masking
Blinded (masking used) (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

Individuals who are 18 years to 45 years old among the staff and students of Universiti Kebangsaan Malaysia (UKM) with no known medical conditions.

Exclusion criteria

1) Neurological deficit (radial nerve symptoms, carpel tunnel) 2) Surgery to elbow previous treatment to elbow including steroid injections within 4 weeks of entering the study. 3) Inflammatory conditions affecting the elbow or wrist 4) Connective tissue disorders 5) Generalized myalgia, neuromuscular diseases 6) Cardiovascular diseases malignancies, haemophilia, diabetes. 7) Prescription medications such as beta-adrenoceptor blocking agents or anti-inflammatory or analgesic drugs 8) History of fracture to humerus, radius, or ulna. 9) Pregnancy 10) Hypermobility syndrome based on The Beighton Score.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 7, 2026