Reaction Time After Mobilization

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

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

66 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-01-07

Study Completion Date

2024-03-02

Brief Summary

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This clinical trial aims to look at the influence of wrist Mulligan mobilizations on hand reaction time in healthy people. The main question it aims to answer is:

1-Do hand mobilizations reduce reaction time?

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Detailed Description

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In the treatment of musculoskeletal problems, manual therapy techniques are often used to restore movement and alleviate pain. The period between the initial muscular response or movement in response to a stimulus is referred to as reaction time. There is growing evidence for the benefit of manual mobilization for limb dysfunction, including shoulder and elbow pain, but there is little literature on hand mobilization and little research on its influence on hand reaction time in healthy individuals.

The study comprised 60 healthy participants who completed a voluntary consent form. They were divided into two groups: research and sham mobilization. Participants in the study group had mediolateral wrist glide, anteroposterior 1st MCP glide, and anteroposterior and mediolateral glide. Applications were performed to the wrist, first metacarpal, and CMC joints in three sets of six repetitions. The patient in the sham mobilization group remained in the same posture for the same amount of time without gliding. The Nelson Hand Reaction Test was used to assess hand reaction before and after application. A 50 cm ruler was used, and the average of five measurements in cm was recorded and interpreted to sec.

Conditions

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Passive Joint Mobilization Reaction Time Immediate Effect

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

They were divided into two groups: research and sham mobilization. Participants in the study group had mediolateral wrist glide, anteroposterior 1st MCP glide, and anteroposterior and mediolateral glide. Applications were performed to the wrist, first metacarpal, and CMC joints in three sets of six repetitions. The patient in the sham mobilization group remained in the same posture for the same amount of time without gliding. The Nelson Hand Reaction Test was used to assess hand reaction before and after application. A 50 cm ruler was used, and the average of five measurements in cm was recorded and interpreted to sec.

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

SINGLE

Participants

Study Groups

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İntervention

In the study group, wrist mediolateral glide, 1st MCP joint anteroposterior glide, CMC joint mediolateral, and anteroposterior glide were applied to the individuals by an experienced physiotherapist. Applications were made 6 times with 3 repetitions

Group Type EXPERIMENTAL

Passive Joint Mobilization

Intervention Type OTHER

Wrist mediolateral glide, 1st MCP joint anteroposterior glide, CMC joint mediolateral, and anteroposterior glide were applied to the individuals. Applications were made 6 times with 3 repetitions

Sham Mobilization

In the sham mobilization group, individuals were placed in the same position, but no mobilization application was performed.

Group Type SHAM_COMPARATOR

Passive Joint Mobilization

Intervention Type OTHER

Wrist mediolateral glide, 1st MCP joint anteroposterior glide, CMC joint mediolateral, and anteroposterior glide were applied to the individuals. Applications were made 6 times with 3 repetitions

Interventions

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Passive Joint Mobilization

Wrist mediolateral glide, 1st MCP joint anteroposterior glide, CMC joint mediolateral, and anteroposterior glide were applied to the individuals. Applications were made 6 times with 3 repetitions

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Volunteers were included if they were 18 years of age or older and had no communication disorders.

Exclusion Criteria

* Any elbow, hand, shoulder, or neck discomfort, diagnosis, or pain in the last 6 months, a neurological disorder affecting sensation, or unwillingness to participate in the study.

Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes