- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02776579
Effect of a Female Strength & Conditioning Specialist on High School Girls' Health
May 2, 2018 updated by: University of Manitoba
Girls in the Weight Room: Assessing the Influence of a Female School-based Strength & Conditioning Specialist on the Health of High School Girls
The majority of today's youth do not engage in enough physical activity (PA) to maintain good health.
Low PA levels are associated with poor health (e.g.
diabetes, high blood pressure) and early mortality.
Girls are less likely than boys to be active, and their rates of participation drop off more steeply during adolescence.
Girls report many barriers to exercise, including transportation issues and feeling self-conscious about their appearance and abilities.
School-based PA programs that try to improve health, mainly through aerobic exercise and education, have had a small effect to date.
However, the few programs that included resistance training as the focus showed strong improvements in health related measures.
In this project, we will examine the effect of a female strength and conditioning specialist on decreasing barriers and increasing the overall health of high school girls, with the delivery of in-school, girls-only resistance training programs.
We will see if physical and mental health changes with the training, and how the presence of the S & C specialist affects the girls' social interactions within the school.
The results will help individuals in the education sector plan programs and services to improve overall youth and school health.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
31
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Manitoba
-
Winnipeg, Manitoba, Canada, R3E 0T6
- University of Manitoba
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
13 years to 18 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Grades 7 to 12 at Grant Park High School
- do not participate on organized sports teams
- self-report as not meeting the recommended amount of 60 min of Moderate-Vigorous Physical Activity per day
Exclusion Criteria:
- engaged in regular resistance training activities within the previous 6 months
- health condition or injury that would put them at risk during testing/training
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Girls-only resistance training
8 weeks of 2-3x/week girls-only resistance training class with a female strength and conditioning specialist.
|
|
No Intervention: No resistance training
8 weeks of usual activity.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
1 Repetition Maximum leg press
Time Frame: Change from Baseline and at 8 weeks
|
Change from Baseline and at 8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
1 Repetition Maximum bench press
Time Frame: Baseline and at 8 weeks
|
Baseline and at 8 weeks
|
|
Grip strength dynamometry
Time Frame: Baseline and at 8 weeks
|
The average of three repetitions for each hand will be used in analysis
|
Baseline and at 8 weeks
|
mCAFT for aerobic fitness
Time Frame: Baseline and at 8 weeks
|
Baseline and at 8 weeks
|
|
Physical activity levels
Time Frame: Baseline and at 8 weeks
|
Average daily minutes spent in Sedentary, Low, Moderate and Vigorous intensity activity over 5 days will be measured via an accelerometer worn around the waist.
|
Baseline and at 8 weeks
|
Physical Self-Perception Profile
Time Frame: Baseline and at 8 weeks
|
36 item questionnaire; scores for embedded scales of "Strength Competence", "Physical Self-Worth", "Global Self-Worth", and "Attractive Body Adequacy" will be calculated.
|
Baseline and at 8 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Joanne Parsons, PhD, University of Manitoba
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 1, 2016
Primary Completion (Actual)
December 1, 2017
Study Completion (Actual)
December 1, 2017
Study Registration Dates
First Submitted
May 9, 2016
First Submitted That Met QC Criteria
May 17, 2016
First Posted (Estimate)
May 18, 2016
Study Record Updates
Last Update Posted (Actual)
May 3, 2018
Last Update Submitted That Met QC Criteria
May 2, 2018
Last Verified
May 1, 2018
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Grant Park
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Physical Inactivity
-
University of Alabama at BirminghamRecruitingDisability Physical | Physical InactivityUnited States
-
University of IowaNational Institute on Aging (NIA); Northeastern UniversityNot yet recruiting
-
Ludwig Boltzmann Institute for Digital Health and...RecruitingPhysical InactivityAustria
-
University of MichiganNational Institute on Aging (NIA)Recruiting
-
University of MinnesotaRecruitingPhysical InactivityUnited States
-
Brown UniversityNational Cancer Institute (NCI)Recruiting
-
Universiti Putra MalaysiaRecruitingInactivity, PhysicalPakistan
-
University of Milano BicoccaFederico II University; University of BergamoRecruitingPhysical InactivityItaly
-
University of CalgaryPublic Health Agency of Canada (PHAC)Recruiting
-
Brown UniversityNational Institute of General Medical Sciences (NIGMS)CompletedPhysical InactivityUnited States
Clinical Trials on Girls-only resistance training
-
University of AlbertaCompletedType 1 DiabetesCanada
-
University of KasselCompleted
-
University of KasselUniversity of PotsdamCompleted
-
University of Alabama at BirminghamCompletedMusculoskeletal and Metabolic CrosstalkUnited States
-
University of Applied Sciences of Western SwitzerlandCompleted
-
University of BarcelonaCompleted
-
Universidade Federal do Triangulo MineiroUnknown
-
Vienna Hospital AssociationRecruiting
-
Universidade Federal de Sao CarlosConselho Nacional de Desenvolvimento Científico e TecnológicoCompletedChronic Obstructive Pulmonary DiseaseBrazil