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NCT07407621Enrolling by invitation

Effects of Short Isokinetic Eccentric Resistance Training on Neuromuscular Induced Adaptations

Effects of Short Isokinetic Eccentric Resistance Training on Neuromuscular Induced Adaptations Among Obese, Untrained Women

Source: ClinicalTrials.gov · Last updated 12 Feb 2026

Brief summary (registry, in English)

The study compares the impact of isokinetic resistance training (RT) -induced neuromuscular adaptation following an 8-week short ECC ISO RT and CON ISO RT among obese, untrained women. The main question it aims to answer is: 1\. Does exercise-induced neuromuscular adaptation following progressive short ECC ISO RT, more effectively than CON ISO RT, among obese, untrained women? Researchers will compare drug ECCISO RT to a CONISO RT to see if ECCISO RT is more effective in inducing neuro-muscular adaptations in obese, untrained women. Participants will: 1. Train on isokinetic ECC or CON for 8 weeks 2. Visit the clinic twice for baseline and post tests

Status (registry)
Enrolling by invitation
Study type
Interventional
Enrollment
24 (estimated)
First submitted
3 Feb 2026
Start date
2 Jan 2025
Primary completion date
1 Mar 2026
Lead sponsor
Universiti Sains Malaysia
Diseases
Obesity
NCT number
NCT07407621

What you commit to

  • Study type: Interventional
  • Planned participants: 24
  • From 2 Jan 2025 to the primary completion date, 1 Mar 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • taking supplements or medication known to affect REE (such as oral contraceptives)
  • suffer from alcohol or drug abuse

Other illness

  • severe medical conditions affecting their physical or mental health

Other

  • smokers
  • individuals with an implanted medical device
  • trying to conceive/ pregnant, or breastfeeding

Who the study is looking for

  • Eumenorrheic women (reporting menstrual cycle between 21-35 days)
  • Age 25-45 y/o
  • BMI \> 23.0 kg/m2
  • Body fat percentage \> 30%
  • No lower limb orthopaedic injuries
  • Have not participated in any structured/ unstructured weight loss intervention in the past 12 months
  • Sedentary lifestyle (regular exercise \<1 hour per week)
  • Stable body weight (loss or gain of no greater than 2 kg)
  • Stable medication use for six months before enrolment

Age in the registry: 18 years to 45 years · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Department of Community Health
Coordinator of this site? Confirm its status
Kepala BatasMalaysiaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.