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Pre-sleep Protein Supplementation in British Army Recruits

Pre-sleep Protein Supplementation Does Not Improve Performance, Body Composition and Recovery in British Army Recruits

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05998590
Enrollment
122
Registered
2023-08-21
Start date
2021-05-01
Completion date
2022-05-31
Last updated
2023-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Protein-energy; Imbalance, Recovery, Body Weight

Brief summary

Dietary protein has been shown to be important to support physical training. For occupational demands such as military training, new recruits often fail to meet the recommended protein intake during basic training (BT), with negligible amounts consumed in the evening. As such, individuals undertaking BT may require higher intakes than the general population.This study assessed the influence of a daily bolus of protein prior to sleep on performance adaptations, body composition and recovery in British Army recruits.

Detailed description

Dietary protein is crucial for optimising physical training adaptations such as muscular strength and mass, which are key aims for athletic populations, including British Army recruits. New recruits fail to meet the recommended protein intake during basic training (BT), with negligible amounts consumed in the evening. This study aimed to assess the influence of a daily bolus of protein prior to sleep on performance adaptations, body composition and recovery in British Army recruits. The study will recruit a mixed cohort of \>120 new recruits from the United Kingdom (UK) British Army who will be randomised into a dietary control (CON), carbohydrate placebo (PLA), moderate (20g) protein (MOD) or high (60g) protein (HIGH) supplementation group. Supplements will be isocaloric and consumed daily on weekday evenings between 2000 and 2100h for 10 weeks during BT, alongside standardised dietary intake and BT activities. Performance tests (mid-thigh pull, medicine ball throw, 2km run time, maximal push-up and maximal vertical jump) and body composition will be assessed at the start and end of BT under standardised conditions. Dietary intake, energy expenditure, salivary hormones, urinary nitrogen balance, perceived muscle soreness, rating of perceived exertion, mood and fatigue will be assessed at the start, middle and end of BT. The underlying aim of this study is to assess whether inclusion of nocturnal protein supplementation will influence performance adaptations, body composition changes or acute recovery in British Army recruits.

Interventions

DIETARY_SUPPLEMENTHigh protein supplement

The participants received a 60g protein bolus each evening prior to sleep from week 3 to week 12 of training.

DIETARY_SUPPLEMENTModerate protein supplement

The participants received a 20g protein bolus each evening prior to sleep from week 3 to week 12 of training.

DIETARY_SUPPLEMENTCarbohydrate placebo

The participants received an isocaloric carbohydrate bolus each evening prior to sleep from week 3 to week 12 of training.

The participants did not receive any supplementation but instead acted as a control group doing BT only

Sponsors

University of Exeter
CollaboratorOTHER
Anglia Ruskin University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Enrolled into British Army basic training * Medically fit to start Army training

Exclusion criteria

* Not taking any other nutritional supplement * Not currently pregnant * Not dairy or lactose intolerant or have any specific dietary requirements .

Design outcomes

Primary

MeasureTime frameDescription
Lower body strength performance12 weeksMid-thigh pull

Secondary

MeasureTime frameDescription
Body composition12 weeksFat-free mass

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026