Dual-Task Effects on Hand Functions in Type 2 Diabetes Mellitus

Kutahya Health Sciences University

Status: Completed

Conditions: Type 2 Diabetes

Treatments: Other: Dual-task

Study type: Interventional

Funder types: Other

Identifiers

NCT05127291

T2DM-Dualtask

Details and patient eligibility

About

The aim of the study is to examine the effect of dual-task performance on hand functions in individuals with Type 2 Diabetes Mellitus. It is planned to reach at least 100 participants during the data collection phase of the study. Demographic information, plasma glucose levels, and HbA1C levels of the participants included in the study will be recorded. The upper extremity problems of the participants will be recorded. Minnesota Manual Dexterity Test will be used to evaluate upper extremity functions.

Full description

This study is aimed to evaluate the effect of dual-task performance on hand functions in individuals with Type 2 Diabetes Mellitus. The study will conduct in the Internal Medicine Clinic of Kutahya Health Sciences University Evliya Celebi Training and Research Hospital. Approval for the study was granted by the Clinical Research Ethics Committee of Kutahya Health Sciences University and written informed consent forms will be obtained from all the participants. This study is planned to reach at least 50 participants with type 2 diabetes mellitus for the study group and 50 participants without diabetes for the control group. The participants will be questioned about their eligibility for the inclusion criteria. The demographic and descriptive data of the participants will be recorded. Minnesota Manual Dexterity Test will be used to evaluate upper extremity functions. The test will be performed with and without the dual-task. Counting backward from a random three-digit number 3 by 3 will be used for the dual-task. The effect of dual-task will calculate using the difference between the completion time of both tests for both groups.

Enrollment: 73 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Having been diagnosed with type 2 diabetes mellitus for at least 5 years for study group, having no diagnosed type 2 diabetes mellitus or prediabetes for control group,
• Being able to count down 3 by 3 from a three-digit number,
• Volunteer to take part in the study.

Exclusion criteria

• History of traumatic or inflammatory injury in the upper extremity,
• History of involving the upper extremity in the last year,
• Having rheumatological/inflammatory arthritis or deformity,
• Having a deformity caused by osteoarthritis in the upper extremity,
• Having a neurological problem affecting the upper extremity,
• Getting 23 points or less on the Mini-Mental Test.

Trial design

Primary purpose: Other

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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73 participants in 2 patient groups

Study Group

Experimental group

Description:

Patients with type 2 diabetes mellitus

Treatment:

Other: Dual-task

Control Group

Other group

Description:

People without type 2 diabetes and prediabetes

Treatment:

Other: Dual-task