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Isometric Exercise for Delayed Onset Muscle Soreness

Effects of Isometric Exercise on Recovery Following Experimentally Induced Delayed Onset Muscle Soreness: A Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07627152
Enrollment
40
Registered
2026-06-04
Start date
2025-04-01
Completion date
2025-07-18
Last updated
2026-06-16

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

Conditions

Delayed Onset Muscle Soreness (DOMS)

Keywords

Isometric Exercise, Exercise-Induced Muscle Damage, Pressure Pain Threshold, Pain, Recovery, Delayed Onset Muscle Soreness (DOMS)

Brief summary

The goal of this clinical trial is to learn whether isometric exercise can improve recovery following experimentally induced delayed onset muscle soreness (DOMS) in healthy young adults. The main questions it aims to answer are: * Does isometric exercise reduce pain associated with delayed onset muscle soreness? * Does isometric exercise improve pressure pain threshold, knee joint range of motion, muscle strength, and recovery following delayed onset muscle soreness? Researchers will compare participants performing an isometric exercise program with a control group receiving no intervention to determine whether isometric exercise improves recovery after experimentally induced DOMS. Participants will: * Undergo a standardized exercise protocol to induce delayed onset muscle soreness. * Be randomly assigned to either an isometric exercise group or a control group. * Complete assessments of pain intensity, pressure pain threshold, knee range of motion, muscle strength, and thigh circumference. * Be evaluated before exercise, immediately after exercise, and on Days 1, 3, and 5 following DOMS induction.

Detailed description

Delayed onset muscle soreness (DOMS) is a common consequence of unaccustomed or high-intensity physical activity, particularly exercises involving eccentric muscle contractions. DOMS is characterized by pain, tenderness, temporary reductions in muscle function, decreased range of motion, and impaired physical performance, typically peaking between 24 and 72 hours after exercise. Various recovery strategies have been investigated to reduce the symptoms of DOMS; however, evidence regarding the effectiveness of isometric exercise in facilitating recovery remains limited. Previous studies have suggested that isometric muscle contractions may induce analgesic effects and increase pressure pain thresholds in musculoskeletal conditions. Whether these effects can improve recovery following exercise-induced muscle damage and DOMS has not been fully established. The purpose of this randomized controlled trial was to investigate the effects of an isometric exercise program on recovery following experimentally induced DOMS in healthy adults. DOMS was induced using a standardized drop-jump protocol. Participants were randomly assigned to either an isometric exercise group or a control group. Outcome assessments were performed before DOMS induction, immediately after exercise, and during follow-up evaluations on Days 1, 3, and 5. The findings of this study may contribute to the understanding of the role of isometric exercise as a simple, low-cost, and clinically applicable recovery strategy following exercise-induced muscle soreness.

Interventions

OTHERIsometric Exercise

Participants performed a structured quadriceps isometric exercise program following experimentally induced delayed onset muscle soreness. The exercise protocol was applied according to the study protocol throughout the recovery period.

Participants performed a sham exercise protocol following experimentally induced delayed onset muscle soreness. The sham intervention was designed to mimic the attention and participation associated with the experimental intervention without providing the intended therapeutic effect.

Sponsors

Istanbul Nisantasi University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Intervention model description

Participants were randomly assigned to either an isometric exercise group or a control group. Delayed onset muscle soreness (DOMS) was induced using a standardized drop-jump protocol. The intervention group performed a structured isometric exercise program, whereas the control group received no intervention. Outcomes were assessed at baseline, immediately after exercise, and on Days 1, 3, and 5 following DOMS induction.

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Active athletes competing in University sports teams. * Age between 18 and 30 years. * Participation in organized sports training at least three times per week for the previous six months. * No lower-extremity pain at the time of enrollment. * Ability to safely perform the exercise protocol used to induce delayed onset muscle soreness (DOMS). * Willingness to provide written informed consent.

Exclusion criteria

* History of lower-extremity musculoskeletal injury within the previous 6 months. * Previous lower-extremity surgery. * Current musculoskeletal pain or injury affecting sports participation. * Neurological, rheumatological, cardiovascular, or systemic disorders affecting physical performance. * Use of analgesic, anti-inflammatory, or muscle-relaxant medications during the study period. * Participation in strenuous eccentric exercise within 72 hours prior to baseline testing. * Use of recovery interventions (e.g., massage, cryotherapy, compression garments, electrical stimulation) during the study period. * Inability to complete the exercise protocol or follow-up assessments.

Design outcomes

Primary

MeasureTime frameDescription
Pressure Pain ThresholdBaseline, immediately after exercise, Day 1, Day 3, and Day 5 following DOMS induction.Pressure pain threshold measured using a digital pressure algometer following experimentally induced delayed onset muscle soreness (DOMS).
Pain IntensityBaseline, immediately after exercise, Day 1, Day 3, and Day 5 following DOMS induction.Pain intensity will be assessed using the Visual Analog Scale (VAS). The VAS consists of a 10-cm horizontal line ranging from 0 (no pain) to 10 (worst imaginable pain). Participants will indicate their perceived pain intensity by marking a point on the line. Higher scores indicate greater pain intensity.

Secondary

MeasureTime frameDescription
Knee Joint Range of MotionBaseline, immediately after exercise, Day 1, Day 3, and Day 5 following DOMS induction.Knee joint range of motion measured using a standard goniometer.
Quadriceps Muscle StrengthBaseline, immediately after exercise, Day 1, Day 3, and Day 5 following DOMS induction.Quadriceps muscle strength measured using a handheld dynamometer.
Thigh CircumferenceBaseline, immediately after exercise, Day 1, Day 3, and Day 5 following DOMS induction.Thigh circumference measured using a tape measure to assess exercise-induced swelling.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 17, 2026