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CompletedNCT02529917Updated May 5, 2017

The Benefits of Hemp Protein Supplementation During Resistance Training

An interventional study of Hemp powder and Soy Powder in Sarcopenia, sponsored by University of Saskatchewan. Completed at 1 site in Canada. Open to participants aged 18 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2017-05-05.

Sponsored by University of Saskatchewan · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
34
Allocation
Randomized
Ages
18 Years to 45 Years
Sex
All
01

Study summary

Forty physically active men and women aged 18-45y will take part in an 8-week resistance training program, randomized (double blind) 1:1 into each of two groups. Twenty participants will be randomized to receive 60 g/d of hemp powder (containing approximately 40 g protein and 9 g oil) supplementation and 20 randomized to receive 60 g/d of soy supplementation (matched to the hemp for macronutrients and calories) during eight weeks of training. Each participant will complete testing before and after the intervention for assessment of body composition (lean tissue, fat, and bone mass), strength, central fatigue, markers of inflammation, and bone resorption. Over the 8-weeks of training, participants will train four-five days per week for 1-1.5 hours per session with exercises targeting all major muscle groups. The training will involve a "two day split" where different muscle groups are trained on two consecutive days (day 1 involves chest, back, and arms; day 2 legs, shoulders, and abdominals). Resistance training will provide the necessary stimulus for protein synthesis to optimize the effect of a protein-containing nutritional supplement. The hemp or soy powder will be consumed in two doses (i.e. 30 g powder containing 20 g protein per dose) immediately after exercise sessions and one hour after exercise. This dosing regimen is optimal for stimulating muscle protein synthesis and building muscle mass . On the one non-training day per week the two doses will be consumed with meals.

02

Conditions studied

  • Sarcopenia

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03

In context

Sarcopenia

1,208 studies on the registry are indexed under Sarcopenia; 402 are open to participants now.

This study's enrollment of 34 is below the median of 60 across 775 interventional studies indexed under Sarcopenia.

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Lead sponsor

University of Saskatchewan is the lead sponsor of 237 studies on the registry; 33 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • At least 6 months experience with resistance training

Exclusion criteria

Exclusion Criteria:

  • Allergies to hemp or soy
  • Consumption of other nutritional supplements in previous month
  • Answered "yes" to questions on the Physical Activity Readiness Questionnaire
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
34 participants (actual)

Study arms

  • Experimental
    Hemp powder

    Hemp powder supplement

    Dietary Supplement: Hemp powder

  • Active comparator
    Soy powder

    Soy powder supplement

    Dietary Supplement: Soy Powder

Interventions

  • Dietary supplementHemp powder

    Hemp powder supplement

  • Dietary supplementSoy Powder

    Soy powder supplement

06

What researchers measure

Primary outcomes

  1. Change in lean tissue mass (kg)

    Lean tissue mass measured with dual energy x-ray absrorptiometry

    Time frame: 8 weeks

Secondary outcomes

  1. Change in fat mass (kg)

    Fat mass as measured by dual energy x-ray absorptiometry

    Time frame: 8 weeks

  2. Change in bone mass (grams)

    Bone mass as measured by dual energy x-ray absorptiometry

    Time frame: 8 weeks

  3. Change in elbow flexor muscle thickness (cm)

    Muscle thickness as assessed by ultrasound

    Time frame: 8 weeks

  4. Change in knee extensor muscle thickness (cm)

    muscle thickness as measured by ultrasound

    Time frame: 8 weeks

  5. Change in bench press strength (kg)

    Bench press strength as assess on a plate-loaded machine by the 1-RM method

    Time frame: 8 weeks

  6. Change in arm curl strength (kg)

    Arm curl strength as assessed with dumbbells by the 1-RM method

    Time frame: 8 weeks

  7. Change in leg press strength (kg)

    Leg press strength as assessed on a leg-press machine by the 1-RM method

    Time frame: 8 weeks

  8. Change in inflammation by interleukin-6 (mmol/l) levels

    Interleukin-6 levels measured from saliva samples

    Time frame: 8 weeks

  9. Change in inflammation by C-reactive protein (mmol/l) levels

    C-reactive protein levels measured from saliva samples

    Time frame: 8 weeks

  10. Change in bone resorption (N-telopeptides) (mmol/l)

    N-telopeptides measured from urine samples

    Time frame: 8 weeks

  11. Change in voluntary muscle activation (Nm)

    Voluntary muscle activation as measured by the interpolated twitch technique

    Time frame: 8 weeks

07

Study locations

1 site
  • University of Saskatchewan
    Saskatoon, Saskatchewan S7N 5B2, Canada
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 5, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02529917
Lead sponsor
University of Saskatchewan
Responsible party
Phil Chilibeck (Ph.D., University of Saskatchewan) — Principal investigator
First posted
Aug 20, 2015
Start date
Aug 2015
Primary completion
Dec 2015
Completion
Dec 2015
Last update
May 5, 2017

Study contacts

Philip Chilibeck
principal investigator · University of Saskatchewan

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2017. You cannot join it, but the record below documents what was studied.

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