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Strength Training With and Without Blood Flow Restriction on Shoulder Muscle Strength in Healthy Adults

A

Alice Maria da Costa Carvalhais

Status

Completed

Conditions

Resistance Training
Blood Flow Restriction (BFR) Training Effects

Treatments

Other: High-load resistance training.
Device: Low-load resistance training with Blood flow Restriction

Study type

Interventional

Funder types

Other

Identifiers

NCT07186231
31/CE-IPSN/2024

Details and patient eligibility

About

The goal of this clinical trial is to compare two types of shoulder strength training: low-load training with blood-flow restriction (BFR) and high-load training without BFR. The study includes healthy adults.

The main questions it aims to answer are:

Are changes in shoulder strength, power, endurance, and muscle mass similar with low-load BFR and high-load training?

Researchers will compare strength training with BFR to strength training without BFR to see whether changes in shoulder muscle performance are similar.

Participants will:

  • Provide basic personal details, body measurements (e.g., height and weight), and a brief medical history before starting.
  • Train in one of the two programs (BFR or no BFR) two times per week for 4 weeks.
  • Complete tests of shoulder maximum strength, power, endurance, and muscle mass at the start and at the end of the protocol.

Full description

All outcome assessments were conducted after a standardized warm-up to minimize measurement variability. The warm-up comprised light aerobic activity, followed by dynamic mobility exercises for the shoulder girdle and upper limbs, and targeted stretching of the shoulder and elbow/forearm muscle groups (two sets of 20-30 seconds per muscle group). Safety procedures included monitoring for adverse symptoms during testing and training; sessions were paused or discontinued according to predefined criteria.

Enrollment

23 patients

Sex

All

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Body Mass Index between 18.5 and 30 kg/m²

Exclusion criteria

  • participation in sports that heavily involve the dominant arm (e.g., tennis, volleyball, or handball) and do not engage in strength training exercises on the upper limb;
  • history of trauma or surgery affecting the dominant upper limb;
  • acute or chronic shoulder pain,;
  • radiating pain;
  • cervical disc herniation;
  • previous neck surgeries,;
  • upper limb edema;
  • history of deep vein thrombosis;
  • history of oncologic or metabolic conditions;
  • pregnancy;
  • experience of persistent symptoms such as numbness, tingling, or pain exceeding 7/10 on a numeric scale during the training (applicable to BFR group);
  • missed more than one session during the study.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

23 participants in 2 patient groups

Low-load strength training with Blood Flow Restriction
Experimental group
Description:
Participants allocated to this study arm, performed a 4-week training with 2 sessions per week, using low load resistance training with Blood Flow Restriction.
Treatment:
Device: Low-load resistance training with Blood flow Restriction
High-load strength training
Active Comparator group
Description:
Participants allocated to this study arm performed 4-week training with 2 sessions per week, using high-load resistance training.
Treatment:
Other: High-load resistance training.

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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