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Creatine or Vitamin D Supplementation in Persons With Spinal Cord Injury Undergoing Resistance Training

U

Universidade do Porto

Status

Completed

Conditions

Spinal Cord Injuries

Treatments

Dietary Supplement: Creatine
Dietary Supplement: Vitamin D
Dietary Supplement: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT02099357
FADEUPAFA20132015

Details and patient eligibility

About

The purpose of this study is to determine the effects of creatine monohydrate or vitamin D supplementation on strength gains following a traditional resistance training program for adults with spinal cord injury.

Enrollment

14 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Spinal cord injury
  • Minimum time since injury: 3 months

Exclusion criteria

  • Participation in resistance training programmes in the previous 6 months
  • Creatine or vitamin D supplementation in the previous 6 months

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

14 participants in 3 patient groups, including a placebo group

Placebo
Placebo Comparator group
Description:
Daily supplementation with 3g of dextrose during eight weeks and placebo ampoules each two weeks.
Treatment:
Dietary Supplement: Placebo
Creatine
Experimental group
Description:
Daily supplementation with 3g of monohydrate creatine during eight weeks. Placebo ampoules each two weeks.
Treatment:
Dietary Supplement: Creatine
Vitamin D
Active Comparator group
Description:
Daily supplementation with 3g of dextrose during eight weeks. Vitamin D supplementation, 25000 IU each two weeks.
Treatment:
Dietary Supplement: Vitamin D

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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