Actively Recruiting

Phase Not Applicable
Age: 65Years +
All Genders
NCT06520995

Elderly Patients With Type 2 Diabetes and Cognitive Exercises

Led by Istanbul University - Cerrahpasa · Updated on 2024-07-25

90

Participants Needed

1

Research Sites

51 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The study was planned as a single-center, prospective randomized controlled study. Individuals over 65 years of age with type 2 diabetes without severe cognitive impairment will be included in the study. The primary aim of the study is to improve the cognitive functions of the patients after the interventions. The secondary aim is to strengthen patients' diabetes self-management and increase their quality of life, especially by improving their glycemic control. For these purposes, in our study, patients will be randomized into three groups: "cognitive exercise and diabetes education", "diabetes education only" and "control" group. The control group will be provided with standard outpatient diabetes education. Individuals who will be in the "cognitive exercise and video training" group will watch a total of 12 diabetes education videos prepared by the researcher, in which a different topic will be discussed every week for 3 months, and they will also participate cognitive exercises for 15-20 minutes a day for 3 months via a mobile application. Individuals in the "diabetes education only" group will similarly watch a total of 12 diabetes education videos prepared by the researchers. Patients will be evaluated in terms of cognitive function, psychosocial problems (anxiety, depression, stress), glycemic control (HbA1c), diabetes management and quality of life before the interventions, at 3 months and 6 months.

CONDITIONS

Official Title

Elderly Patients With Type 2 Diabetes and Cognitive Exercises

Who Can Participate

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with type 2 diabetes for at least one year
  • Literate
  • Able to use smartphone/tablet/computer and have internet access
  • Individuals who agree to participate in the study will be included.
Not Eligible

You will not qualify if you...

  • Type 1 diabetes
  • Severe cognitive impairment
  • Known neurological or psychiatric disorders
  • Severe depression
  • Individuals with disabilities such as vision or hearing problems

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Istanbul University-Cerrahpasa, Florence Nightingale Faculty of Nursing

Istanbul, Avcılar, Turkey (Türkiye), 34320

Actively Recruiting

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Research Team

H

Hande Bulut Canbaz, RN,Msc

CONTACT

Z

Zeliha Tulek, RN,Prof.Dr.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

3

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