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Change in grip strength induced by overflow contralateral to hip flexion

Change in grip strength induced by overflow contralateral to hip flexion

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-2dx9m4h
Enrollment
Unknown
Registered
2025-05-03
Start date
2023-01-20
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Healthy Volunteers

Interventions

This is a two-arm, double-blind, randomized controlled trial with a total of 90 participants, 45 in the control group and 45 in the treatment group. Control Group (CG): Individuals in this group will
G11.427.410.698.277

Sponsors

Universidade de São Paulo
Lead Sponsor
Universidade de São Paulo
Collaborator

Eligibility

Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: They were aged between 18 and 30 and had a motor preference for the right upper limb.

Exclusion criteria

Exclusion criteria: Volunteers with orthopaedic alterations, pain, difficulty in performing the palmar grasp and hip flexion movements, and failure to achieve at least 70 per cent of the maximum hip flexion force.

Design outcomes

Primary

MeasureTime frame
Expected outcome 1: We hope to identify whether muscle strength irradiation techniques, induced by resisted isometric contraction of the hip flexors at 70% of the maximum voluntary isometric contraction, could positively interfere with the handgrip strength measured contralaterally. ;Expected outcome 2: It was hoped to observe an attenuation of the progressive reduction in strength over multiple repeated maximal tests.;Outcome found 1: Strength maintenance was more evident in the test phase, suggesting that the contralateral irradiation resulting from isometric hip flexion mitigated neuromuscular fatigue in the upper limbs.;Outcome found 2: It was observed that the participants in the irradiation group showed a significant attenuation in the reduction of handgrip strength (p < 0.05) during the maximum repeated tests, compared to the control group.

Secondary

MeasureTime frame
No secondary outcomes were expected

Countries

Brazil

Contacts

Public ContactGustavo Rosa

Universidade de São Paulo

gustavohenrique@usp.br+5516993234370

Outcome results

None listed

Source: REBEC (via WHO ICTRP)