Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06368128

Climbing Lifestyle Intervention for Modifying Physical Activity Behaviors: Pilot Study

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).

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year–35 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Northern Michigan University

Marquette, Michigan, 49855, United States

Location status: Recruiting

Location contact

Lisa Eckert, PhD

CONTACT

[email protected]

906-227-1291

Megan C Nelson, PhD

PRINCIPAL_INVESTIGATOR

About this study

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).

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Indoor Rock Climbing Exercise Training Program

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.

Primary outcomes

  1. 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

  2. Fasting glucose

    Time frame: 0, 6, 12, 24 weeks

    glucose (mg/dL) measured via capillary blood sample and point-of-care testing

  3. Hemoglobin a1c

    Time frame: 0, 6, 12, 24 weeks

    Glycosylated hemoglobin (%) measured via capillary blood sample and point-of-care testing

Secondary outcomes

  1. Physical activity and sedentary behavior

    Time frame: 0, 6, 12, 24 weeks

    Objectively monitored light, moderate, and vigorous physical activity minutes per week

  2. Sedentary behavior bouts (30 min, 60 min, >60 min)

    Time frame: 0, 6, 12, 24 weeks

    Objectively monitored number of bouts of sedentary behavior occurring in bouts of 30 minutes or less, 30-60 minutes, and greater than 60 minutes

  3. Cardiorespiratory fitness

    Time frame: 0, 12 weeks

    VO2max (mL/kg/min) measured via expired air analysis

  4. Muscular fitness

    Time frame: 0, 12 weeks

    Maximal isometric handgrip strength (kg) using an electronic handgrip dynamometer

  5. Handgrip strength asymmetry

    Time frame: 0, 12 weeks

    Maximal isometric handgrip strength measured using an electronic handgrip dynamometer on both hands

  6. Lower-body dynamic balance

    Time frame: 0, 12 weeks

    Lower-quarter y-balance test distance (cm) on each leg, in the anterior, posteromedial, and posterolateral directions.

  7. Health-related quality of life using CDC Health-Related Quality of Life Scale

    Time frame: 0, 6, 12, 24 weeks

    Core healthy days module, activity limitations module. Core healthy days module measures the number of days over the past 30 days where injury, mental health, was not good and kept individuals from performing usual activities. Activity limitations asks if individuals are limited by any health problems, how many days they are limited by health problems, and if needs are impaired. Healthy days symptom module asks if pain, depression, anxiety and sleep were an issue on any number of days over the past 30 days. Additionally, how many days individuals felt healthy and full of energy over the past 30 days.

  8. Exercise self-efficacy measured via Self-efficacy for exercise scale

    Time frame: 0, 6, 12, 24 weeks

    Self-efficacy for exercise scale is 9 items representing various scenarios that are measured on a scale of 1 (not confident) to 10 (very confident) a participant feels to exercise in that scenario. Higher scores represent higher self-efficacy for exercise participation.

  9. Perceptions of exercise measured via Views and Attitudes Toward Exercise Scale

    Time frame: 0, 6, 12, 24 weeks

    Views and attitudes towards exercise scale is 15 items measured on a 7-point Likert scale from strongly disagree (lowest) to strongly agree (highest). Sum up all responses, higher scores are better perceptions of exercise.

  10. Perceived stress

    Time frame: 0, 6, 12, 24 weeks

    Perceived stress scale items are scored from adding up each alternative over 10 items: 0=never, 1=almost never, 2=sometimes, 3=fairly often, 4=very often. 0-13=low stress, 14-26=moderate stress, 27-40=high perceived stress.

  11. Blood pressure

    Time frame: 0, 6, 12, 24 weeks

    Systolic and diastolic blood pressure (mmHg) measured via automated blood pressure cuff.

  12. Body composition

    Time frame: 0, 12, 24 weeks

    Fat free mass, fat mass in kg using Dual-energy x-ray absorptiometry

  13. Bone density

    Time frame: 0, 12, 24 weeks

    Total bone density (g/cm3) using Dual-energy x-ray absorptiometry

Study contacts

Contact information is provided by the study sponsor or research team.

Lisa Eckert, PhD

CONTACT

[email protected]

906-227-1291

Sponsors and collaborators

Lead sponsor

Northern Michigan University

Other

Registry information

Official study title

Climbing Lifestyle Intervention for Modifying Physical Activity Behaviors (CLIMB): Pilot Study

Acronym: CLIMB

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Apr 16, 2024
Registry last updated
Jul 16, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.