EMS Recovery Effects in Sport Climbing

NCT ID: NCT07336745

Last Updated: 2026-01-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-01-10

Study Completion Date

2021-07-10

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Sport climbing often requires athletes to perform repeated climbing efforts with short rest periods. Over time, fatigue can build up in the muscles of the arms and forearms, which may reduce performance and increase the difficulty of continuing to climb at the same level.

This study aims to better understand different recovery methods that climbers may use between climbing efforts. Specifically, the study compares two recovery approaches: electrical muscle stimulation-based recovery and passive recovery (resting while seated).

In this study, adult male sport climbers will complete a structured climbing task designed to induce fatigue. After the climbing task, participants will receive one of the two recovery methods. On a separate study visit, they will complete the same procedure using the other recovery method. The order of the recovery methods will be randomized, and there will be a break of one week between sessions.

During the study sessions, researchers will record climbing-related performance measures, simple strength and endurance tasks, heart rate, and how hard the participants feel they are working. The information collected will help researchers better understand recovery strategies used in climbing and may inform training and recovery practices for athletes in the future.

Participation in the study is voluntary, and all procedures are conducted under controlled laboratory conditions.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Sport climbing places high and repetitive demands on the forearm muscles, which are required to sustain repeated gripping and pulling actions with limited recovery time. During prolonged or repeated climbing bouts, local muscular fatigue can accumulate, potentially affecting endurance and movement quality. Competitive climbers are particularly exposed to these demands, as competitions often involve multiple rounds performed within the same day with short rest intervals. For this reason, recovery strategies that can be applied between climbing efforts are of practical relevance in both training and competition settings.

Electrical muscle stimulation (EMS) is a recovery modality that delivers low-intensity electrical impulses to skeletal muscle, producing rhythmic, involuntary contractions. EMS has been used in various sport and rehabilitation contexts as a low-effort method that can be applied without additional mechanical load. However, its application as an inter-bout recovery strategy in sport climbing has not been sufficiently characterized under controlled, climbing-specific conditions.

This study is designed as a randomized crossover trial to compare EMS-based recovery (EMSr) and passive recovery (PASr) following a standardized climbing fatigue protocol. Advanced male sport climbers will participate in two experimental sessions separated by a one-week washout period. In each session, participants will complete the same climbing fatigue protocol, followed by one of the two recovery conditions, with the order of recovery methods randomized.

The fatigue protocol consists of repeated climbing bouts performed on a standardized training wall using a fixed route of defined difficulty. This protocol is intended to elicit localized forearm fatigue under reproducible conditions. Following completion of the fatigue protocol, participants will undergo either EMS applied to the forearm muscles for a fixed duration or passive recovery involving seated rest without additional intervention.

Climbing-related performance measures, muscular endurance tasks, cardiovascular responses, and ratings of perceived exertion will be recorded at predefined time points before and after the recovery period. These measurements are included to characterize physiological and performance-related responses associated with each recovery condition.

The crossover design allows each participant to serve as their own control, thereby reducing inter-individual variability and enabling a direct comparison of recovery approaches under standardized conditions.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Exercise-Induced Fatigue Forearm Muscle Fatigue

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

EMS Recovery (EMSr) Arm

Participants completed a standardized climbing fatigue protocol consisting of 15 sets of 1-minute climbs followed by 1-minute rest on a TensionBoard route (IRCRA grade 15). Immediately after the fatigue protocol, participants underwent Electrical Muscle Stimulation-based Recovery (EMSr). EMS was applied to the forearm flexor muscles (flexor carpi radialis, palmaris longus, flexor carpi ulnaris) using a Chattanooga Wireless Professional 4CH device with 5×5 cm electrodes. The "Active Recovery" program (2-4-6-5-4-3-2-1 Hz; 50 minutes) was used. Stimulation intensity was individually adjusted to elicit visible muscle contraction without discomfort.The EMSr intervention was designed to facilitate local muscle recovery, maintain climbing-specific performance (total move count, isometric hang time), and reduce performance decrements compared to passive rest.

Group Type EXPERIMENTAL

Electrical Muscle Stimulation

Intervention Type DEVICE

This intervention specifically targets the forearm flexor muscles (flexor carpi radialis, palmaris longus, flexor carpi ulnaris) using low-frequency electrical stimulation to promote local muscle recovery after climbing-induced fatigue. The protocol uses a 50-minute "Active Recovery" program (2-4-6-5-4-3-2-1 Hz) applied via a device, with intensity individually adjusted to elicit visible muscle contraction without discomfort. Unlike general active recovery or passive rest, this intervention provides localized neuromuscular stimulation designed to preserve climbing-specific performance metrics such as total move count and weighted isometric hang time.

Passive Recovery (PASr) Arm

Participants completed the same standardized climbing fatigue protocol (15 × 1-minute climbs with 1-minute rest on a TensionBoard route, IRCRA grade 15). Immediately after the fatigue protocol, participants underwent passive recovery (PASr), consisting of 50 minutes of seated rest. No active muscle stimulation or exercise was performed during this period.

The PASr arm serves as a control condition to evaluate the effects of EMS-based recovery on climbing-specific performance metrics.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Electrical Muscle Stimulation

This intervention specifically targets the forearm flexor muscles (flexor carpi radialis, palmaris longus, flexor carpi ulnaris) using low-frequency electrical stimulation to promote local muscle recovery after climbing-induced fatigue. The protocol uses a 50-minute "Active Recovery" program (2-4-6-5-4-3-2-1 Hz) applied via a device, with intensity individually adjusted to elicit visible muscle contraction without discomfort. Unlike general active recovery or passive rest, this intervention provides localized neuromuscular stimulation designed to preserve climbing-specific performance metrics such as total move count and weighted isometric hang time.

Intervention Type DEVICE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Male climbers aged 30-36 years.
* At least 3 years of continuous climbing experience, training 3-4 times per week.
* Ability to climb at least IRCRA grade 15 (French 6a) routes.
* In good general health and able to safely perform high-intensity climbing.
* Willing to provide written informed consent and follow study instructions.

Exclusion Criteria

* Participation in other sports with high training loads that could interfere with the study.
* Any injury, medical condition, or musculoskeletal problem that limits climbing performance.
* Use of medications or supplements that could affect muscle performance or recovery.
* Inability to comply with study procedures, including the climbing and recovery protocols.
Minimum Eligible Age

18 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Akdeniz University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Akdeniz University Faculty of Sport Sciences

Antalya, , Turkey (Türkiye)

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

TSA-2019-4786

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Effects of Muscle Fatigue
NCT07009496 COMPLETED NA