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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.
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.
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Live Instruction and Fitness Tracking (LIFT-up) | Behavioral | A 12-week combined aerobic and resistance training exercise protocol |
| Measure | Description | Time Frame |
|---|---|---|
| Bodyweight as assessed by InBody H20N | 2.5 pound weight change from baseline | 12 weeks |
| Waist circumference as assessed by tape measure 1-in above umbilicus | change waist circumference from baseline | 12 weeks |
| Body Composition as assessed by Bod Pod | change fat mass from baseline | 12 weeks |
| Body Mass Index as assessed by InBody H20N | change body mass index from baseline | 12 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| 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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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| LaShawn Nastvogel, Ph.D. | University of Maryland Eastern Shore | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Maryland Eastern Shore | Princess Anne | Maryland | 21853 | United States |
I do not wish to share individual participant data.
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP_ICF | Yes | Yes | Yes | Study Protocol, Statistical Analysis Plan, and Informed Consent Form | Feb 23, 2023 | Sep 25, 2023 | Prot_SAP_ICF_000.pdf |
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| ID | Term |
|---|---|
| D057185 | Sedentary Behavior |
| D000073599 | Health Risk Behaviors |
| ID | Term |
|---|---|
| D001519 | Behavior |
| D015438 | Health Behavior |
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