NCT06196099

Brief Summary

The current research landscape shows studies indicating increased muscle strength and hypertrophy through neuromuscular electrical stimulation combined with blood flow restriction. However, there is a lack of research specifically on the effects of this combination during rest periods. Therefore, the primary objective of this study is to investigate the impact of resting blood flow restriction training combined with neuromuscular electrical stimulation on blood lactate levels and changes in lower limb muscle function in healthy male adults.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
12

participants targeted

Target at below P25 for not_applicable healthy

Timeline
Completed

Started Dec 2023

Shorter than P25 for not_applicable healthy

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 23, 2023

Completed
7 days until next milestone

Study Start

First participant enrolled

December 30, 2023

Completed
10 days until next milestone

First Posted

Study publicly available on registry

January 9, 2024

Completed
2 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 11, 2024

Completed
19 days until next milestone

Study Completion

Last participant's last visit for all outcomes

January 30, 2024

Completed
Last Updated

January 23, 2025

Status Verified

January 1, 2025

Enrollment Period

12 days

First QC Date

December 23, 2023

Last Update Submit

January 20, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Blood lactate

    Lactate levels were measured using the Accutrend Plus (Roche, Germany). A small amount of whole blood was collected from the participants for blood lactate concentration analysis. The procedure involved the finger-prick method, where the tip of the right index finger was disinfected with an alcohol swab. Then, a lancet prepared for this purpose was used to obtain a small sample of capillary blood from the disinfected area. The collected blood was then applied to lactate strips, and the blood lactate analyzer (Accutrend Plus, Roche, Germany) provided the lactate level readings within 60 seconds.

    Immediate change from baseline after intervention

Study Arms (3)

rest-Blood Flow Restriction plus Neuromuscular Electrical Stimulation

ACTIVE COMPARATOR
Device: Blood Flow RestrictionDevice: Neuromuscular Electrical Stimulation

rest-Blood Flow Restriction

ACTIVE COMPARATOR
Device: Blood Flow Restriction

Squat Exercise

ACTIVE COMPARATOR
Behavioral: Squat exercise

Interventions

The study participants were instructed to rest quietly in a seated position for 10 minutes. During the last 3 minutes of the resting period, upper arm blood pressure was measured twice using an automatic blood pressure monitor (BP170, InBody, Korea). The blood flow restriction cuffs (BFR Therapy Cuff, BFR Therapy Co., USA) - measuring 5cm in width and 60cm in length - were applied to the upper third of the thigh on both legs. To maintain consistency in measurements, the distance from the proximal part of the kneecap to the distal edge of the cuff was measured. A Capillary Reaction Time (CRT) test was used to assess the appropriateness of the cuff pressure; this involved applying thumb pressure to the quadriceps muscle after cuff application and timing how long it took for the skin color to return to normal.

rest-Blood Flow Restrictionrest-Blood Flow Restriction plus Neuromuscular Electrical Stimulation

Neuromuscular Electrical Stimulation (NMES) was applied five times a week for one week using a four-channel stimulator (Compex Physio, Chattanooga, Switzerland). The stimulation protocol was set to a frequency of 35Hz, with electrodes attached to the vastus lateralis and vastus medialis muscles. The therapist adjusted the intensity and alternating output of the electrodes selectively to facilitate the squat exercises required during the intervention. During the stimulation period, participants were engaged in a squat exercise program, with the total duration of stimulation being 10 minutes.

rest-Blood Flow Restriction plus Neuromuscular Electrical Stimulation
Squat exerciseBEHAVIORAL

In this study, the squat exercise was performed in four sets. Participants were instructed to position their feet shoulder-width apart and educated to squat in such a way that their knees did not extend beyond their toes. To ensure consistency in performing the squat at the same angle, a mark was made on the wall at the pelvic height during a 90° squat. This allowed participants to perform squats at the same height. The exercise was conducted under the guidance of a physical therapist with five years of clinical experience.

Squat Exercise

Eligibility Criteria

Age20 Years - 29 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Healthy adult males in their 20s,
  • Individuals who answered less than one item on the PAR-Q (Physical Activity Readiness Questionnaire),
  • Participants who consented to the use and publication of their physical function evaluation data and expressed a desire to participate in the exercise experiment.

You may not qualify if:

  • Individuals with severe hypertension (blood pressure above 170/110 mmHg),
  • Individuals with a history of deep venous thrombosis,
  • Individuals with endothelial dysfunction,
  • Individuals with peripheral vascular disease,
  • Individuals with one or more of the following conditions: diabetes, infection, cancer,
  • Participants who expressed a desire to withdraw during the study period or whose participation rate was below 80% were excluded from the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Honam University

Gwangju, 62399, South Korea

Location

MeSH Terms

Interventions

Blood Flow Restriction Therapy

Intervention Hierarchy (Ancestors)

Exercise TherapyRehabilitationAftercareContinuity of Patient CarePatient CareTherapeuticsPhysical Therapy Modalities

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Investigator

Study Record Dates

First Submitted

December 23, 2023

First Posted

January 9, 2024

Study Start

December 30, 2023

Primary Completion

January 11, 2024

Study Completion

January 30, 2024

Last Updated

January 23, 2025

Record last verified: 2025-01

Data Sharing

IPD Sharing
Will share

Locations