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Impact of Electrical Stimulation during Exercise on healthy Individuals: pilot study

Effects of High-frequency Transcutaneous Electrical Nerve Stimulation during Resisted Exercise on pain and function in healthy individuals: a pilot randomized crossover clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-9zbhcrx
Enrollment
50
Registered
2026-06-03
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Patellofemoral Pain Syndrome Knee Injuries

Interventions

This is a randomized crossover pilot clinical trial with random allocation and double blind masking involving the evaluator and the participants. The study will include 50 healthy individuals allocate

Sponsors

Universidade Federal do Delta do Parnaíba
Lead Sponsor
Universidade Federal do Delta do Parnaíba
Collaborator

Eligibility

Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Healthy individuals; university students; of both sexes; aged between 18 and 35 years; with no pain complaints or history of knee injuries; irregularly active and sedentary; who have not performed resistance training of the lower limb musculature for two months prior to the study; must present a body mass index (BMI) of less than 30 kg/m²

Exclusion criteria

Exclusion criteria: Present with any musculoskeletal, rheumatologic, cardiovascular, neurological, or systemic disorder that could be exacerbated by strenuous exercise; have received a corticosteroid knee injection within the last 6 months; have undergone previous ankle, knee, or hip surgery; have had any experience with Transcutaneous Electrical Nerve Stimulation (TENS) or have any contraindication that prevents the use of electrostimulation, such as an allergy to the electrode material; cardiac pacemaker use; pregnancy; epilepsy; altered skin conditions, or loss of sensitivity in the areas designated for electrode placement

Design outcomes

Primary

MeasureTime frame
It is expected to find an increase in the pressure pain threshold of the participants, verified by a digital algometer, based on the observation of an increase in the supported pressure (measured in kPa) in the post-intervention assessments (performed immediately after, 10, 20, and 30 minutes after the intervention) compared to the initial baseline measurement

Secondary

MeasureTime frame
It is expected to observe an improvement in physical function, verified by means of the single leg horizontal jump functional test, based on the finding of the average distance reached in centimeters in three valid jump attempts comparing the moments before and after the intervention

Countries

BR

Contacts

Public ContactGlauko Dantas

Universidade Federal do Delta do Parnaíba

glauko.dantas@ufdpar.edu.br+55(86)99451-0372

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Jun 29, 2026