Climbing Lifestyle Intervention for Modifying Physical Activity Behaviors: Pilot Study

NCT ID: NCT06368128

Last Updated: 2024-07-16

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 12 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-04-16
• Study Completion Date: 2024-12-31

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).

Conditions

Lifestyle Factors; Physical Inactivity; Quality of Life

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

Control

Participants in the control arm will be asked to maintain their current lifestyle behaviors.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Intervention

Participants in the intervention arm will be asked to partake in a 12-week progressive, supervised, indoor rock climbing training program.

Group Type: EXPERIMENTAL

Indoor Rock Climbing Exercise Training Program

Intervention Type: BEHAVIORAL

Training will occur 2-3 days per week for 60 minutes; ratings of perceived exertion between 3-7 on a scale of 0-10 will be targeted for the desired intensity throughout the program. Minutes of rock climbing will also be monitored to develop the progression strategy.

Interventions

Indoor Rock Climbing Exercise Training Program

Training will occur 2-3 days per week for 60 minutes; ratings of perceived exertion between 3-7 on a scale of 0-10 will be targeted for the desired intensity throughout the program. Minutes of rock climbing will also be monitored to develop the progression strategy.

Intervention Type: BEHAVIORAL

Eligibility Criteria

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

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 35 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Northern Michigan University

OTHER

Sponsor Role: lead

Responsible Party

Megan C. Nelson

Assistant Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Megan C Nelson, PhD

Role: PRINCIPAL_INVESTIGATOR

Northern Michigan University

Locations

Northern Michigan University

Marquette, Michigan, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

Lisa Eckert, PhD

Role: CONTACT

leckert@nmu.edu

906-227-1291

Facility Contacts

Lisa Eckert, PhD

Role: primary

leckert@nmu.edu

906-227-1291

Other Identifiers

HS-24_51

Identifier Type: -

Identifier Source: org_study_id