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Recruiting NCT07433686

Saskatoon Berry Juice for Muscle Recovery

No phase Interventional Muscle Damage

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Dietary Supplement, Placebo.
Who it may be relevant to
Registry conditions: Muscle Damage. Basic parameters: 18 years — 35 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Canada
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Effect of Short-term Saskatoon Berry Supplementation on Muscle Recovery

Overview

This study will evaluated the effect of Saskatoon berry juice on recovery from muscle-damaging exercise.

Detailed description

Saskatoon berries are high in polyphenols which are are anti-inflammatory and act as anti-oxidants. They therefore have potential to protect muscle from damage induced by intense exercise. Thirty participants will be randomized to receive Sasaktoon berries (375 ml) or placebo every day for 10 days. On the seventh day participants will perform 6 sets of intense biceps curl exercise. Isometric muscle strength, muscle swelling, and muscle soreness will be assessed before exercise, immediately after exercise, and 24, 48, and 72 hours after the exercise session. We hypothesize the group receiving Saskatoon berries will have faster recovery of muscle strength, and reduction in swelling and muscle soreness after the exercise session.

Interventions

  • Dietary supplement Dietary Supplement
    Saskatoon berries (375 ml)
  • Dietary supplement Placebo
    Placebo (375 ml)

Primary outcome measures

  • Change in isometric biceps strength with a dynamometer (Nm) [Time frame: 72 hours]
Secondary outcome measures (2)
  • Change in biceps muscle thickness with ultrasound (cm) [Time frame: 72 hours]
  • Change in muscle soreness with visual analog scale (score ranges from 0 to 10). No soreness = 0, maximal soreness = 10 [Time frame: 72 hours]

Eligibility criteria

Inclusion criteria

  • Male or female
  • aged 18-35y

Exclusion criteria

  • Conditions that might be affects by exercise as determined by the "Get Active Questionnaire"

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Triple blind
Primary purpose
Treatment

Study locations

Canada · 1 center
  • Physical Activity Complex, University of Saskatchewan — Saskatoon

Identifiers

NCT: NCT07433686 · 006

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗