Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06024577
Other study ID # 2023-152
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 18, 2023
Est. completion date July 2028

Study information

Verified date September 2023
Source California Polytechnic State University-San Luis Obispo
Contact Todd Hagobian, PhD
Phone 8057567511
Email thagobia@calpoly.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Only 50% of sedentary adults that start an exercise training program adhere to the program after 6 months. Exercise variety may improve adherence. The goal of this study is to examine different exercise interventions that include a variety of exercise on adherence.


Description:

Regular exercise, in the form of walking 150 minutes per week, is widely regarded as having many health and fitness benefits. Despite these well-known benefits, adherence to exercise interventions is extremely low. When sedentary adults start an exercise training program only 50% adhere to the program and meet the national recommendations of 150 minutes per week. A possible explanation of the low adherence is that most adults only walk for exercise, and that providing a variety of exercise may increase adherence. Preliminary observational data show that a variety of exercise may increase weekly exercise expenditure compared to other interventions. The overall objective of this study is to investigate the feasibility, adherence, and acceptability of different exercise interventions including 1) walk intervention, 2) variety intervention, and 3) progressive intervention (see below for description).


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date July 2028
Est. primary completion date July 2027
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - 18-40 years old - Sedentary (<1 hour per week of exercise) - BMI 18.5 to 40 kg/m2 Exclusion Criteria: - Adults with diagnosed cardiovascular, diabetes, renal, or any other metabolic disease determined by Health and Fitness History questionnaire. - Any other disability, ailment, or physical characteristics that may hinder the ability to participate in regular exercise determined by Health and Fitness History questionnaire. - Participating in other studies that would interfere with their ability to safely complete the exercise protocols. - Pregnant or trying to become pregnant, and peri-menopausal or post-menopausal women. - History of smoking within the last 6 months - Any other vulnerable population (children <18, pregnant women, prisoners, etc.)

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Walking
Prescribed 150 minutes per week of moderate to vigorous walking.
Variety
Prescribed 150 minutes per week of moderate to vigorous variety of exercise. Each week participants are randomly asked to participate in cycling, walking/jogging, yoga/Pilates, or cross-training.
Progressive
Prescribed 150 minutes per week of moderate to vigorous progressive variety of exercise. Each week participants are randomly asked to participate in cycling, walking/jogging, yoga/Pilates, or cross-training. Participants can choose which exercise they want to do, and can do as much or little as they want.

Locations

Country Name City State
United States California Polytechnic State University San Luis Obispo California

Sponsors (1)

Lead Sponsor Collaborator
California Polytechnic State University-San Luis Obispo

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Adherence to exercise intervention Adherence is assessed as meeting or exceeding 150 minutes per week of moderate to vigorous exercise Change from baseline at 1-week, 2-weeks, 3-weeks, and 4-weeks
Secondary Acceptability of intervention Participants will complete a survey on acceptability at the end of the exercise intervention Acceptability at 4-weeks
Secondary Body Weight Body weight will be measured at baseline and 4-weeks Change in body weight from baseline to 4-weeks
See also
  Status Clinical Trial Phase
Completed NCT03643432 - Adherence for Exercise Rehabilitation in Older People Trial N/A
Recruiting NCT03464331 - Promoting Zero-time Exercise in Patients With Coronary Heart Disease N/A
Not yet recruiting NCT05057416 - The Effect of Exercise Intensity on Adherence N/A
Completed NCT05481190 - The Impact Of A Tele-Exercise Program For Children With Cystic Fibrosis During The Covid-19 Pandemic On Quality Of Life N/A
Completed NCT04784793 - Postural Alignment Exercise Mobile App for Cervical and Thoracic Spine Regions N/A
Completed NCT00281437 - Health First-Study 2 Phase 2/Phase 3