Climbing Lifestyle Intervention for Modifying Physical Activity Behaviors: Pilot Study
CLIMB
1 other identifier
interventional
12
1 country
1
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).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Apr 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 18, 2024
CompletedFirst Posted
Study publicly available on registry
April 16, 2024
CompletedStudy Start
First participant enrolled
April 16, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2024
CompletedJuly 16, 2024
July 1, 2024
9 months
March 18, 2024
July 15, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Fasting lipids
HDL-c; LDL-c; total cholesterol, triglycerides measured via capillary blood sample and point-of-care testing
0, 6, 12, 24 weeks
Fasting glucose
glucose (mg/dL) measured via capillary blood sample and point-of-care testing
0, 6, 12, 24 weeks
Hemoglobin a1c
Glycosylated hemoglobin (%) measured via capillary blood sample and point-of-care testing
0, 6, 12, 24 weeks
Secondary Outcomes (13)
Physical activity and sedentary behavior
0, 6, 12, 24 weeks
Sedentary behavior bouts (30 min, 60 min, >60 min)
0, 6, 12, 24 weeks
Cardiorespiratory fitness
0, 12 weeks
Muscular fitness
0, 12 weeks
Handgrip strength asymmetry
0, 12 weeks
- +8 more secondary outcomes
Study Arms (2)
Control
NO INTERVENTIONParticipants in the control arm will be asked to maintain their current lifestyle behaviors.
Intervention
EXPERIMENTALParticipants in the intervention arm will be asked to partake in a 12-week progressive, supervised, indoor rock climbing training program.
Interventions
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.
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Northern Michigan University
Marquette, Michigan, 49855, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Megan C Nelson, PhD
Northern Michigan University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
March 18, 2024
First Posted
April 16, 2024
Study Start
April 16, 2024
Primary Completion
December 31, 2024
Study Completion
December 31, 2024
Last Updated
July 16, 2024
Record last verified: 2024-07
Data Sharing
- IPD Sharing
- Will not share
This is a small pilot study; individual participant data will not be shared to protect participants information so that it remains confidential.