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Comparison of the Effects of Motor and Cognitive Dual Task Exercises on Fall Risk, Balance, and Gait

2026年9月11日 更新者:Bihter Aslanyurek、Ankara Yildirim Beyazıt University

Comparison of the Effects of Motor and Cognitive Dual Task Exercises on Fall Risk, Balance, and Gait in Geriatric Individuals Residing in Nursing Homes: A Randomized Controlled Trial

This study aimed to compare the effects of motor and cognitive dual-task exercise programs on fall risk, balance, and gait performance in older adults residing in nursing homes.The main question it aims to answer is:

An eight-week motor or cognitive dual-task exercise program did not provide additional benefits over standard single-task exercise in improving fall risk, balance, or gait performance in nursing home residents.

All interventions were administered for approximately 40 minutes per session, three times per week, for eight weeks.

Assessments were conducted before and after the intervention using the Five-Repetition Sit-to-Stand Test, 2-Minute Walk Test, Single-Leg Stance Test, Timed Up and Go (TUG) Test, Tinetti Balance and Gait Scale, and Functional Reach Test.

調査の概要

詳細な説明

Individuals residing in nursing homes who were aged between 65 and 95 years, able to walk independently, literate, willing to participate, and cognitively capable of understanding and performing the assessments and exercises were included in the study.

Individuals with systemic or metabolic conditions such as malignancy, osteoporosis, history of fracture, coagulation disorders, active infection, orthostatic hypotension, or pacemaker implantation were excluded. Participants were withdrawn from the study if they discontinued the intervention, failed to attend pre- or post-intervention assessments, or were unable to understand or perform the required tests and exercises.

A total of 69 eligible participants were allocated into three groups using a systematic allocation sequence based on the order of enrollment. Participants were assigned sequentially to the motor dual-task group, cognitive dual-task group, or control group in a 1:1:1 ratio.

Due to the absence of a dedicated exercise room, all interventions were conducted in participants' rooms using space-adapted exercise protocols.

Participants in the motor dual-task group performed a structured exercise program consisting of the Five Times Sit-to-Stand Test, Timed Up and Go test (3 m), single-leg stance, 10-meter tandem walking, 10-meter normal walking, and a 20-meter marching activity while simultaneously carrying a tray filled with water.

Participants in the cognitive dual-task group performed the same exercise program combined with a concurrent cognitive task. During each exercise, participants were instructed to verbally generate proper nouns beginning with the letter "A".

The control group performed a conventional exercise program of equivalent duration and frequency without any additional dual-task component.

All interventions were administered for approximately 40 minutes per session, three times per week, for eight weeks.

Baseline demographic characteristics, including participant identification number, group allocation, age, sex, body weight, and height, were recorded using a standardized assessment form. All evaluations were performed before and after the eight-week intervention period by the same physiotherapist to ensure assessment consistency and minimize inter-rater variability.

Fall risk was assessed using the Five Times Sit-to-Stand Test (FTSST). Balance and gait performance were evaluated using the 2-Minute Walk Test (2MWT), Single-Leg Stance Test, Timed Up and Go (TUG) Test, Tinetti Balance and Gait Assessment Scale, and Functional Reach Test.

研究の種類

介入

入学 (実際)

69

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • ÇANKAYA
      • Ankara、ÇANKAYA、トルコ(Türkiye)、06550
        • Altınçatı Nursing Home and Elderly Care Center

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 高齢者

健康ボランティアの受け入れ

はい

説明

Inclusion Criteria:

  • residing in nursing homes who were aged between 65 and 95 years
  • Individuals able to walk independently
  • Individuals who are literate
  • Individuals willing to participate in the study
  • Individuals cognitively capable of understanding and performing the required assessments and exercises.

Exclusion Criteria:

  • Individuals with malignancy
  • Individuals with osteoporosis
  • Individuals with a history of fracture
  • Individuals with coagulation disorders
  • Individuals with an active infection
  • Individuals with orthostatic hypotension
  • Individuals with pacemaker implantation

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:独身

武器と介入

参加者グループ / アーム
介入・治療
アクティブコンパレータ:対照群
The control group performed a conventional exercise program of equivalent duration and frequency without any additional dual-task component. All interventions were administered for approximately 40 minutes per session, three times per week, for eight weeks.
実験的:Motor Dual-Task Exercise Group
Participants in the motor dual-task group performed a structured exercise program consisting of the Five Times Sit-to-Stand Test, Timed Up and Go test (3 m), single-leg stance, 10-meter tandem walking, 10-meter normal walking, and a 20-meter marching activity while simultaneously carrying a tray filled with water. All interventions were administered for approximately 40 minutes per session, three times per week, for eight weeks.
実験的:Cognitive Dual-Task Exercise Group
Participants in the cognitive dual-task group performed the same exercise program combined with a concurrent cognitive task. During each exercise, participants were instructed to verbally generate proper nouns beginning with the letter "A". All interventions were administered for approximately 40 minutes per session, three times per week, for eight weeks.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
2-Minute Walk Test (2MWT)
時間枠:8 weeks
Walking capacity was assessed over a 30-meter walkway during a two-minute period. Participants wore comfortable clothing and footwear and rested for 10 minutes before testing. The total walking distance was recorded in meters.
8 weeks
Five Times Sit-to-Stand Test (FTSST)
時間枠:8 weeks
The FTSST was used to assess lower extremity strength, functional mobility, and fall risk. Participants were instructed to stand up from a standard chair and sit down five consecutive times as quickly as possible while keeping their arms crossed over the chest. Total completion time was recorded using a stopwatch.
8 weeks
Timed Up and Go (TUG) Test
時間枠:8 weeks
Functional mobility was assessed by measuring the time required for participants to stand up from a chair, walk 3 meters, turn around, return to the chair, and sit down. Time was recorded in seconds using a stopwatch.
8 weeks

二次結果の測定

結果測定
メジャーの説明
時間枠
Single-Leg Stance Test
時間枠:8 weeks
Static balance was evaluated by asking participants to stand on one leg while lifting the opposite foot approximately 5 cm off the ground. Participants were instructed to maintain balance for as long as possible, and the duration was recorded using a stopwatch.
8 weeks
Tinetti Balance and Gait Assessment Scale
時間枠:8 weeks
Balance and gait performance were assessed using the Tinetti Balance and Gait Assessment Scale according to standardized administration procedures. Total scores were used to classify fall risk.
8 weeks
Functional Reach Test
時間枠:8 weeks
Dynamic balance was assessed using the Functional Reach Test. A measuring tape was positioned horizontally on the wall at shoulder height. Participants were instructed to reach forward as far as possible with the dominant arm elevated to 90° shoulder flexion without stepping or losing balance. The distance between the initial and maximal reach positions was recorded in centimeters.
8 weeks

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

捜査官

  • 主任研究者:BİHTER AKINOĞLU, Assoc. Prof. Dr., PT.、Ankara Yildirim Beyazıt University

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2023年11月25日

一次修了 (実際)

2024年9月15日

研究の完了 (実際)

2024年11月25日

試験登録日

最初に提出

2026年9月11日

QC基準を満たした最初の提出物

2026年9月11日

最初の投稿 (実際)

2026年9月16日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月16日

QC基準を満たした最後の更新が送信されました

2026年9月11日

最終確認日

2026年9月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

IPD プランの説明

The datasets generated and analyzed during the current study are not publicly available due to ethical and privacy restrictions involving older adult participants residing in nursing homes. The data presented in this study are available on request from the corresponding author.

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米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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