Climbing Lifestyle Intervention for Modifying Physical Activity Behaviors (CLIMB): Pilot Study
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- Northern Michigan University
- Enrollment
- 12
- Locations
- 1
- Primary Endpoint
- Hemoglobin a1c
Study Overview
Brief Summary
The aim of this pilot study is to determine the effects of a 12-week indoor rock climbing training program on heart health, mental health, and behavioral health in generally healthy adults aged 18-35 years old who do not exercise. Participants will learn to rock climb using ropes on an indoor rock climbing wall and participate in the training program 2-3 days per week for 60 minutes each session over 12 weeks. Health outcomes will be measured at 4 time points over the course of the study (pre-intervention, 6-weeks/mid-intervention, 12-weeks/post-intervention, and 24-weeks post-intervention).
Detailed Description
The purpose of this study is to determine the effects of a 12-week progressive, supervised indoor rock climbing intervention on physical, mental, and behavioral health outcomes in physically inactive adults. This will be a pilot study used for informing a larger, randomized controlled trial. Measurements include: cardiometabolic disease risk factors (e.g., blood pressure, fasting glucose and lipids, hemoglobin a1c), health-related components of physical fitness (e.g., cardiorespiratory fitness, muscular fitness, dynamic balance, body composition), health-related quality of life, and behavior change variables (e.g., attitudes toward physical activity, self-efficacy for exercise, objective physical activity and sedentary behavior). The majority of rock climbing-related studies focus on enhancing performance in high-level climbing athletes and very little research has examined the specific impact of climbing physical activity on cardiovascular health parameters. Indoor climbing has demonstrated to be an activity that is safe for many individuals and does not require a high level initial fitness to partake in the activity. This study will engage generally healthy, physically inactive adults (aged 18-35 y) in an indoor rock climbing program 2 times per week for 60 minutes for the first 4 weeks and progressing to 3 times per week for 60 minutes for the last 8 weeks. Participants will partake in top-rope style rock climbing and bouldering. Data collection will occur over three visits to the School of Health and Human Performance Research Lab at four time points throughout the course of the study (baseline/pre-intervention, 6-weeks/mid-intervention, 12-weeks/post-intervention, 24-weeks post-intervention; total of 12 data collection visits).
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Prevention
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to 35 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Physically inactive
- •Membership to Physical Education Instructional Facility at Northern Michigan University
- •No/very little experience with rock climbing
- •No diagnosed cardiovascular, metabolic, renal disease
- •No current injury
Exclusion Criteria
- •Physically active
- •Experience with rock climbing
- •No current membership with Physical Education Instructional Facility at Northern Michigan University
- •Pregnant and/or breastfeeding
- •Diagnosis of cardiovascular disease, metabolic disease, renal disease
- •Current or previous injury that would be exacerbated by rock climbing
- •Other diagnosed conditions in which rock climbing would be contraindicated
Arms & Interventions
Control
Participants in the control arm will be asked to maintain their current lifestyle behaviors.
Intervention
Participants in the intervention arm will be asked to partake in a 12-week progressive, supervised, indoor rock climbing training program.
Intervention: Indoor Rock Climbing Exercise Training Program (Behavioral)
Outcomes
Primary Outcomes
Hemoglobin a1c
Time Frame: 0, 6, 12, 24 weeks
Glycosylated hemoglobin (%) measured via capillary blood sample and point-of-care testing
Fasting lipids
Time Frame: 0, 6, 12, 24 weeks
HDL-c; LDL-c; total cholesterol, triglycerides measured via capillary blood sample and point-of-care testing
Fasting glucose
Time Frame: 0, 6, 12, 24 weeks
glucose (mg/dL) measured via capillary blood sample and point-of-care testing
Secondary Outcomes
- Physical activity and sedentary behavior(0, 6, 12, 24 weeks)
- Cardiorespiratory fitness(0, 12 weeks)
- Lower-body dynamic balance(0, 12 weeks)
- Bone density(0, 12, 24 weeks)
- Sedentary behavior bouts (30 min, 60 min, >60 min)(0, 6, 12, 24 weeks)
- Muscular fitness(0, 12 weeks)
- Exercise self-efficacy measured via Self-efficacy for exercise scale(0, 6, 12, 24 weeks)
- Blood pressure(0, 6, 12, 24 weeks)
- Health-related quality of life using CDC Health-Related Quality of Life Scale(0, 6, 12, 24 weeks)
- Handgrip strength asymmetry(0, 12 weeks)
- Perceptions of exercise measured via Views and Attitudes Toward Exercise Scale(0, 6, 12, 24 weeks)
- Perceived stress(0, 6, 12, 24 weeks)
- Body composition(0, 12, 24 weeks)
Investigators
Megan C. Nelson
Assistant Professor
Northern Michigan University
