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Beta-lactoglobulin, Immobilisation and Muscle Protein Synthesis

K

King's College London

Status

Enrolling

Conditions

Muscle Atrophy

Treatments

Dietary Supplement: Beta-lactoglobulin
Dietary Supplement: Carbohydrate

Study type

Interventional

Funder types

Other

Identifiers

NCT05496452
BLGIMMPS

Details and patient eligibility

About

The objectives of this study are to:

  1. Establish whether combined β-lactoglobulin supplementation and resistance training for 1 week prior to 5 days of limb immobilisation will attenuate the decrease in integrated free-living rates of MPS during short-term muscle disuse.
  2. Establish whether combined β-lactoglobulin supplementation and resistance training for 1 week prior to limb immobilisation will attenuate the decrease in muscle mass and strength during short-term muscle disuse.

Full description

The objectives of this study are to:

  1. Establish whether combined β-lactoglobulin supplementation and resistance training for 1 week prior to 5 days of limb immobilisation will attenuate the decrease in integrated free-living rates of MPS during short-term muscle disuse.
  2. Establish whether combined β-lactoglobulin supplementation and resistance training for 1 week prior to limb immobilisation will attenuate the decrease in muscle mass and strength during short-term muscle disuse.

Hypotheses

  1. Combining β-lactoglobulin and resistance training for 1 wk prior to 5 d of limb immobilisation will attenuate the decrease in integrated muscle protein synthesis, muscle fibre CSA, quadriceps muscle strength, and leg lean mass during muscle disuse.
  2. Combining β-lactoglobulin and resistance training for 1 wk prior to 5 d of limb immobilisation will attenuate the decrease in muscle fibre CSA, quadriceps muscle strength, and leg lean mass during muscle disuse.

Enrollment

24 estimated patients

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Male and female
  • Aged 18-45 years
  • Healthy
  • Physically active (≥150-300 minutes of moderate-intensity aerobic physical activity per week OR 75-150 minutes of vigorous-intensity aerobic physical activity per week)
  • Eumenorrheic and not taking any hormonal birth control (females)

Exclusion criteria

  • Dairy allergy or intolerance
  • Lower limb injury or surgery in the last 6 months,
  • Lower limb osteoarthritis or other musculoskeletal disorder
  • A musculoskeletal or blood blotting disorder
  • An allergy to local anaesthetic
  • Currently pregnant
  • Current use of blood thinning medications
  • Volunteers that take part in structured resistance exercise training
  • Taking supplements considered to be anabolic to skeletal muscle (protein supplements, creatine, or omega-3 supplements)
  • Consuming more than 1.2 grams of protein per kilogram of body mass per day in their habitual diet.
  • Volunteers involved in other studies at the time of enrolment
  • Volunteers who have taken part in a tracer study in the past 18 months
  • If without an understanding of verbal or written English
  • Volunteers with a history of eating disorders

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

24 participants in 2 patient groups, including a placebo group

Beta-lactoglobulin
Experimental group
Description:
Daily supplementation over 12 day period. A nutritional supplement.
Treatment:
Dietary Supplement: Beta-lactoglobulin
Carbohydrate
Placebo Comparator group
Description:
Daily supplementation over 12 day period. Energy matched control.
Treatment:
Dietary Supplement: Carbohydrate

Trial contacts and locations

1

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Central trial contact

Alix Hughes, MSc; Oliver C Witard, PhD

Data sourced from clinicaltrials.gov

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