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Completed

NCT Number: NCT06329388

Evaluating the Effects of an Oral Protein Supplement on Children's Growth Patterns

This single-center, randomized controlled pilot study aims to evaluate the efficacy of TruHeight Growth Protein Shake on improving growth patterns in children aged 4-17 years. Over six months, participants will consume the protein shake daily, five times a week, with outcomes measured in terms of type X collagen concentration in urine, height via a stadiometer, and body composition using an INBODY device.

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Key information

Age range

4 year–17 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

SF Research Institute

San Francisco, California, 94127, United States

About this study

This single-center pilot clinical trial was conducted for TruHeight to determine the effect of oral protein supplement (Growth Protein Shake-GPS) versus control on growth patterns in children. The hypothesis posits that GPS protein supplementation will improve growth patterns as assessed by the concentration of collagen X in the urine, height as measured by a stadiometer, as well as weight and body composition as measured by an INBODY device in six months.

The oral supplement was provided in powder form, which could be mixed with water before consumption.

Participants were recruited from the SF RESEARCH INSTITUTE database and through advertisements on social media and public places. Initial attendance at SF RESEARCH INSTITUTE marked the baseline study visit, where subjects underwent screening for eligibility based on the Inclusion and Exclusion Criteria. Upon meeting qualification criteria, enrollees were assigned a subject number sequentially as they joined the study. A total of 32 subjects, aged 4-17 years, embarked on the study, targeting a completion cohort of 20. Randomization into either the treatment/supplement group or control group occurred via a computer-generated code.

The trial comprised three study visits (SV) over a 6-month period. Measurements of height, weight, fat mass, and lean body mass took place at baseline (SV1), 3 months ± 5 days (SV2), and 6 months ± 5 days (SV3). Urine samples collected at SV1 and SV3 underwent laboratory analysis for type X collagen content. Depending on the group assignment, a dietary or consumer perception questionnaire was provided to be completed by the participant or the participant's guardian at baseline, SV2, and SV3. Treatment group participants or their guardians received a log form to document supplement intake at home. Maintenance of regular diet throughout the study was mandatory for all participants.

Instructions for subjects in the treatment/supplement group were as follows:

Mix and consume two (2) scoops of the dietary supplement with 12-16 fluid oz of water daily, five times per week, for 6 months. The investigator initiated follow-up calls to subjects or their guardians on day 45 (between SV1 and SV2) and day 120 (between SV2 and SV3) to assess compliance with the study protocol.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Children aged 4-17 years old
  • At or below the 50th percentile for height according to CDC growth charts
  • Able to consume the protein shake
  • Willing to maintain their regular diet throughout the study

Exclusion criteria

  • Known allergies to ingredients in the protein shake
  • Currently receiving growth hormone therapy
  • Any medical condition that can affect growth or requires special diet

Treatment and study plan

TruHeight Growth Protein Shake

Dietary Supplement

Participants will be administered two scoops of TruHeight Growth Protein Shake, mixed with 12-16 fluid ounces of water, once daily, five times per week for six months. The supplement is intended to support growth patterns in children by providing essential nutrients that contribute to bone development and overall growth.

Primary outcomes

  1. Change in Height

    Time frame: 6 months

    The primary measure is the difference in children's height measured by a stadiometer from baseline to the end of the study at six months.

Secondary outcomes

  1. Change in Type X Collagen Concentration in Urine

    Time frame: Baseline and 6 months

    Measure the difference in Type X collagen concentration in urine samples from baseline to the end of the study to assess bone growth.

  2. Change in Body Composition

    Time frame: Baseline, 3 months, and 6 months

    Evaluate the difference in body composition, including fat mass and lean body mass percentage, using the INBODY device from baseline to the end of the study.

  3. Incidence of Adverse Events

    Time frame: Throughout the study period of 6 months

    Monitor and record any adverse events experienced by participants throughout the study duration.

Sponsors and collaborators

Lead sponsor

TruHeight Vitamins

Industry

Collaborators

  • San Francisco Research Institute

Registry information

Official study title

A Six-Month Randomized Controlled Pilot Study Evaluating the Effects of an Oral Protein Supplement on Children's Growth Patterns

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
Mar 25, 2024
Registry last updated
Mar 26, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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