Factors Associated With Cognitive Status in the Elderly

Sponsor
Pamukkale University (Other)
Overall Status
Completed
CT.gov ID
NCT05051319
Collaborator
(none)
814
1
36.6
22.2

Study Details

Study Description

Brief Summary

The aim of this study was to investigate the factors related to cognitive status in elderly individuals living in the community. A total of 841 elderly (female: 422, male: 419) living in the community were included in this cross-sectional study. The sociodemographic information of the elderly was recorded. In addition, cognitive status, quality of life, depression and musculoskeletal pain were questioned. The classification and regression tree analysis was used to identify factors associated with cognitive status. Age, depression, quality of life, neck pain, and headache were determinative on the cognitive status of the elderly. Knowing the factors related to cognitive status in elderly individuals living in the community is very important in terms of early diagnosis of factors that may affect the quality of life of these individuals.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Aim: The aim of this study was to investigate the factors related to cognitive status in elderly individuals living in the community.

    Methods: A total of 841 elderly (female: 422, male: 419) living in the community were included in this cross-sectional study. The sociodemographic information of the elderly was recorded. In addition, cognitive status, quality of life, depression and musculoskeletal pain were questioned. The classification and regression tree analysis was used to identify factors associated with cognitive status.

    Study Design

    Study Type:
    Observational [Patient Registry]
    Actual Enrollment :
    814 participants
    Observational Model:
    Other
    Time Perspective:
    Cross-Sectional
    Official Title:
    Investigation of Factors Associated With Cognitive Status in the Elderly
    Actual Study Start Date :
    Apr 1, 2017
    Actual Primary Completion Date :
    Feb 11, 2019
    Actual Study Completion Date :
    Apr 20, 2020

    Arms and Interventions

    Arm Intervention/Treatment
    Elderly participants living at home

    Participants over the age of 65, living at home, not having mental and communication problems that would prevent the evaluations, and volunteering to participate in the study. The sociodemographic information of the participants such as gender, duration of education, living environment and people with whom they live were recorded. In addition, information about the medical condition of geriatric individuals, such as body mass indexes and the number of drugs used, was also recorded in the form. In order to evaluate the cognitive status of the participants, the Standardized or Standardized Mini-Mental Test for the Uneducated was used according to their educational status. The Center for Disease Control Health-Related Quality of Life-4 Scale (CDC HRQoL-4) was used to assess quality of life, and the Geriatric Depression Scale was used to assess emotional status. In addition, the presence of pain and pain levels according to body regions were determined with a 6-point Likert-type scale.

    Outcome Measures

    Primary Outcome Measures

    1. Center for Disease Control and Prevention Health-Related Quality of Life-4 Scale [Two years]

      The quality of life of the elderly participants was evaluated with the first question of the CDC HRQOL-4 scale. The Turkish validity-reliability study of the scale is a short and understandable scale used to evaluate the quality of life. This scale consists of 4 questions evaluating the general health of the participants, their physical and mental health in the last 30 days, and how activities such as self-care, work, school, and hobbies have been affected by their physical or mental problems in the last 30 days. In question 1, general health was defined as excellent, very good, good, fair, and poor. In the 2nd, 3rd, and 4th questions, the number of days in the last 30 days when the participant felt unwell physically and mentally, and the number of days the person could not perform his daily activities due to physical and/or mental problems are recorded.

    2. Standardized Mini-Mental Test [Two years]

      Standardized Mini-Mental Test was applied to determine the cognitive levels of the participants. For the illiterate elderly, SMMT, which is used for the uneducated, was applied in our study. In this test, orientation (10 points), recording memory (3 points), attention and calculation (5 points), recall (3 points) and language (9 points) were collected under 5 main headings. It consists of 11 items and is evaluated over a total of 30 points. Results; 27-30 points are within normal limits, 24-27 points are mild cognitive impairment, below 24 points are considered severe cognitive impairment. The Turkish validity and reliability study of the questionnaire was conducted in 2002.

    3. Geriatric Depression Scale [Two years]

      The scale was prepared for the geriatric individuals to easily mark and answer "yes" or "no". It consists of 30 questions. In the scoring of the scale, 1 point is given for each response in favor of depression and 0 point is given for the other answer, and the result is accepted as the depression score. Scoring of the scale was made as "no depression" with 0-10 points, "possible depression" with 11 points, and "definite depression" with 14 and above points. When 14 is taken as the threshold value for Geriatric Depression Scale scores, its specificity approaches 100%. A validity and reliability study of the Geriatric Depression Scale was conducted in the Turkish elderly population.

    4. Assessment of Pain [Two years]

      The chronic pain status in 10 different body regions of the individuals were assessed in the study. The presence of pain (present or absent) and severity of pain in geriatric individuals were evaluated with a 6-point Likert-type scale (0=no pain, 1=mild, 2=moderate, 3=severe, 4=very severe, 5=unbearable). This pain scale was preferred in order to make it easier for geriatric individuals to understand the severity of pain.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    65 Years and Older
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    • Participants over the age of 65,

    • Living at home,

    • Not having mental and communication problems that would prevent the evaluations,

    • Volunteering to participate in the study.

    Exclusion Criteria:
    • Central nervous system diseases affecting cognitive functions.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Pamukkale University Denizli Kınıklı/Pamukkale Turkey 20070

    Sponsors and Collaborators

    • Pamukkale University

    Investigators

    • Principal Investigator: Güzin Kara, Pamukkale University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Güzin Kara, Principal Investıgator, Pamukkale University
    ClinicalTrials.gov Identifier:
    NCT05051319
    Other Study ID Numbers:
    • 60116787-020/16528
    First Posted:
    Sep 21, 2021
    Last Update Posted:
    Sep 21, 2021
    Last Verified:
    Sep 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No

    Study Results

    No Results Posted as of Sep 21, 2021