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Study on the Effects of Low-to-Mid Frequency Electrical Stimulation on Recovering from Delayed Onset Muscle Soreness (DOMS)

Study on the Effects of Low-to-Mid Frequency Electrical Stimulation on Recovering from Delayed Onset Muscle Soreness (DOMS)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600127289
Enrollment
Unknown
Registered
2026-06-29
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

Delayed Onset Muscle Soreness

Interventions

Medium-Frequency Electrical Stimulation:Electrical stimulation intervention lasting 30 minutes was performed once daily immediately after acid-inducing exercise, at 24 h and 48 h. Electrodes were atta
Low-frequency electrical stimulation:Electrical stimulation intervention lasting 30 minutes was performed once daily immediately after acid-inducing exercise, at 24 h and 48 h. Electrodes were attache
Placebo Control Group:Electrical stimulation intervention was administered once daily for 30 minutes immediately after exercise, at 24 hours and 48 hours post-exercise. Electrodes were attached to the

Sponsors

Beijing Sport University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Having the habit of irregular high-intensity exercise (engaging in moderate-intensity exercise < 3 times a week). 2.Being able to cooperate in completing the experimental process. 3.Signing the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Contraindications to electrical stimulation (including cardiac pacemaker, skin damage or allergies, and history of epilepsy). 2.Any musculoskeletal, neurological, metabolic, or cardiovascular system diseases. 3.Taking anti-inflammatory drugs, analgesics, or muscle relaxants within the past 3 months or during the experiment. 4.Intake of caffeine or alcohol within 48 hours before the experiment.

Design outcomes

Primary

MeasureTime frame
visual analogue scale (VAS) for muscle pain;maximal voluntary contraction (MVC) of the quadriceps;

Secondary

MeasureTime frame
Likert Scale for Muscle Soreness (0–6 points);pressure pain threshold;muscle thickness via musculoskeletal ultrasound;knee flexion range of motion;Endurance ratio (total work of last 5 reps / first 5 reps at 180°/s);blood lactate concentration;

Countries

China

Contacts

Public ContactShi Huiran

Beijing Sport University

2024210380@bsu.edu.cn+86 157 3738 0823

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026