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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06063837
Other study ID # 11-2022-004
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 24, 2023
Est. completion date April 28, 2023

Study information

Verified date September 2023
Source University of Maryland Eastern Shore
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This project was a 12-week aerobic and resistance training intervention that included participants meeting at a pre-determined location from 1-2 times per week for 12 weeks. Aerobic activity was walking. Resistance training included traditional and non-traditional implements.


Description:

The 12-week program included a 60-minute session. Participants filled out a Physical Activity Readiness Questionnaire and completed pre-exercise fitness tests. The fitness tests included the curl up, pushup, and a 1.5 mile walk test. The session involved a warmup which included stretching followed by a 5-min walk for a total of 10 minutes. Functional bodyweight and resistance training exercises were implemented and supervised by the principal investigator (PI) who specializes in program design and implementation. The exercises targets major muscle groups such as legs, chest, back, and shoulders. The resistance training portion took 30-35 minutes. Steady-state aerobic activity which included walking took place at the end of the session for 10-15 minutes. The intensity was monitored using self-rated RPE scores which participants would report to the PI following each session.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date April 28, 2023
Est. primary completion date April 13, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Somerset county resident - Pass American College of Sports Medicine (ACSM) screening algorithm 2022 and the Physical activity readiness questionnaire Exclusion Criteria: - signs/symptoms of cardiovascular, metabolic or renal disease without medical clearance

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Live Instruction and Fitness Tracking (LIFT-up)
A 12-week combined aerobic and resistance training exercise protocol

Locations

Country Name City State
United States University of Maryland Eastern Shore Princess Anne Maryland

Sponsors (1)

Lead Sponsor Collaborator
University of Maryland Eastern Shore

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Bodyweight as assessed by InBody H20N 2.5 pound weight change from baseline 12 weeks
Primary Waist circumference as assessed by tape measure 1-in above umbilicus change waist circumference from baseline 12 weeks
Primary Body Composition as assessed by Bod Pod change fat mass from baseline 12 weeks
Primary Body Mass Index as assessed by InBody H20N change body mass index from baseline 12 weeks
Secondary Cardiorespiratory endurance for time and heart rate as assessed by the Rockport 1-mile Fitness Walking Test equation for estimating cardiorespiratory fitness change estimated VO2 max from baseline 12 weeks
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