Actively Recruiting

Phase Not Applicable
Age: 40Years - 65Years
All Genders
Healthy Volunteers
ID05567237

Effects of Microcurrent Treatment With and Without Resistance Exercises on Body Composition, Muscle Strength, and Physical Function in Middle-aged Adults

Led by University of Greenwich · Updated on 2024-07-24

40

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effects of microcurrent treatment alone and combined with a resistance exercise program on muscle strength, body composition, and physical function in middle-aged adults who are not regularly trained. This study uses a randomized, balanced, double-blind design to compare four groups: microcurrent alone, microcurrent with resistance training, sham treatment alone, and sham treatment with resistance training. The goal is to understand how microcurrent therapy may help counteract age-related muscle decline and improve wellbeing in sedentary adults aged 40 to 65. Participants will be assigned to either receive a microcurrent or sham device, and can choose to participate in a supervised resistance training program or be in a non-exercise group. The resistance training involves elastic bands and includes two sessions per week over six weeks, with exercises targeting the whole-body musculature. The microcurrent or sham device will be worn on the dominant upper arm for three hours daily, either after training or in the mornings on non-training days for those exercising, or every morning for non-exercisers. Throughout the study, researchers will measure body composition using plethysmography, muscle thickness with ultrasound, strength, functional capacity, and blood markers related to health and wellbeing before and after the six-week intervention. Participants' exercise intensity will be monitored using a perceived exertion scale. The study will also consider participants' preferences for training in a group setting or at home via video sessions. The total study period includes a familiarization phase followed by 6 weeks of intervention and assessments at baseline and post-intervention.

CONDITIONS

Brief Title

Effects of Microcurrent Treatment With and Without Resistance Exercises

Who Can Participate

Age: 40Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 40 to 65 years
  • Non-regularly trained male and female adults
Not Eligible

You will not qualify if you...

  • Musculoskeletal injuries
  • Metabolic conditions or diseases
  • Currently taking medications, smoking, or using nutritional supplements known to affect physical performance, muscle damage, or recovery within 6 weeks prior to the study

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Familiarization

Duration - Up to 1 week

Participants who will undergo resistance training complete 2 supervised sessions to learn exercises and control intensity before starting the main intervention.

2 visits (in-person or supervised online)

Treatment

Duration - 6 weeks

Participants receive either microcurrent or sham treatment daily, with some groups also performing resistance training two times per week for 6 weeks.

12 training sessions (in-person or online) for exercise groups; daily device use for all participants

Follow-up Assessments

Duration - 1 to 2 days

Participants have measurements taken to assess changes in body composition, muscle thickness, and blood health markers after the intervention period.

2 visits (before and after treatment)

Trial Site Locations

Total: 1 location

1

School of Human Sciences, University of Greenwich, Avery Hill Campus, Sparrows Farm

London, United Kingdom, SE9 2BT

Actively Recruiting

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Research Team

F

Fernando Naclerio, PhD

S

Stefan Kolimechkov, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

4

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