NCT06368128

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

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
12

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Apr 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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

Completed
29 days until next milestone

First Posted

Study publicly available on registry

April 16, 2024

Completed
Same day until next milestone

Study Start

First participant enrolled

April 16, 2024

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2024

Completed
Last Updated

July 16, 2024

Status Verified

July 1, 2024

Enrollment Period

9 months

First QC Date

March 18, 2024

Last Update Submit

July 15, 2024

Conditions

Keywords

Rock ClimbingCardiovascular Disease Risk FactorsPhysical InactivityQuality of Life

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 INTERVENTION

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

Intervention

EXPERIMENTAL

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

Behavioral: Indoor Rock Climbing Exercise 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.

Intervention

Eligibility Criteria

Age18 Years - 35 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

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

RECRUITING

MeSH Terms

Conditions

Sedentary Behavior

Condition Hierarchy (Ancestors)

Behavior

Study Officials

  • Megan C Nelson, PhD

    Northern Michigan University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Lisa Eckert, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: Randomized controlled trial with participants allocated to either a control or intervention group; comparison between groups and within groups
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.

Locations