このページは自動翻訳されたものであり、翻訳の正確性は保証されていません。を参照してください。 英語版 ソーステキスト用。

The Effects of Somatic-Based Chair Exercises in the Elderly

2026年5月25日 更新者:İlkay Tuğçe Köse、Istanbul Gedik University

The Effects of Somatic-Based Chair Exercises on Balance, Pain, and Quality of Life in the Elderly

The primary aim of this study is to investigate the effects of easily applicable somatic-based chair exercises on balance and pain in the elderly. Additionally, the study aims to reveal the impact of exercise on functionality and cognitive level, and the resulting changes in quality of life.

The main research questions addressed in this study are:

  • What are the most suitable exercise models that can be applied to improve pain control and balance in the elderly?
  • How do the results of different approaches aimed at improving the quality of life in the elderly differ?

調査の概要

詳細な説明

Somatic education refers to a process of sensory-motor learning that enables individuals to develop greater conscious control over their physiological functions. In this study, Thomas Hanna's definition of somatics and Hanna Somatic Education will be used. Thomas Hanna (1976) introduced the term "somatics" to describe the discipline of movement reeducation (somatic education/somatic movement), which aims to promote inner awareness of an individual's body. The practice of somatic movement involves pandiculation. Pandiculation is a process that starts with deliberate muscle activation and transitions into a slow and controlled eccentric release. This is done with ongoing sensory focus, and the movements remain gentle, unforced, and require little effort.

The study design involves comparing the effects of structured somatic-based chair exercises with the effects of a conventional exercise method consisting of basic range of motion exercises combined with static stretching.

研究の種類

介入

入学 (推定)

70

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。

研究連絡先

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:

  1. 65 years of age or older
  2. To be volunteered to participate
  3. To be able to speak and understand Turkish at a good level

Exclusion Criteria:

  1. Scoring <24 on the Mini-Mental State Examination
  2. Any neurological or orthopedic problem that would prevent the implementation of assessment and exercise methods

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:支持療法
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Somatic-based Chair Exercise Group
This group will participate in a structured somatic-based chair exercise program. The program will last for 8 weeks, with sessions held twice a week, each lasting 35 to 40 minutes.
The intervention includes a structured somatic-based chair exercise program (SSCE) developed in accordance with Thomas Hanna's somatic education approach. The program consists of gentle, slow, and controlled movements incorporating pandiculation techniques to improve body awareness and movement control. Exercises target multiple body regions, including the neck, trunk, pelvis, shoulders, upper and lower extremities, wrists, hips, and ankles. Sessions will be performed twice weekly for 8 weeks, with each session lasting approximately 35-40 minutes. A total of 35 volunteers will be enrolled in the SSCE.
他の名前:
  • Structured Somatic-Based Chair Exercises
  • SSCE
アクティブコンパレータ:Conventional Exercise Group
The conventional exercise group will participate in a program that combines static stretching and range of motion (ROM) exercises. The exercise program will last for 8 weeks, with sessions held twice a week, each lasting 35 to 40 minutes.
A total of 35 volunteers will be enrolled in the conventional exercise program, which combines range of motion (ROM) exercises and passive stretching of the same body regions and muscle groups as those addressed in the somatic exercise group.

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
Pain Assessment
時間枠:1 week before the study (T0); at week 4 (T1) and at week 8 (T2)
Pain will be assessed via the Brief Pain Inventory (BPI). BPI measures two objectives: the subjective severity of pain and the causal effect of pain. The questions include numerical rating scales from 0 to 10 (0: none; 1-4: mild; 5-6: moderate, and 7-10: severe).
1 week before the study (T0); at week 4 (T1) and at week 8 (T2)
Balance Ability Assessment
時間枠:1 week before the study (T0); at week 4 (T1) and at week 8 (T2)

Balance ability will be assessed by using the Berg Balance Test (BBT).

The BBT measures balance ability (static and dynamic) among older adults. It is a qualitative measure that assesses balance by performing functional activities such as reaching, bending, transferring, and standing, including most components of postural control. The test contains 14 items. A higher score indicates better balance and a lower risk of falling.

1 week before the study (T0); at week 4 (T1) and at week 8 (T2)
Objective Balance Assessment via Becure Balance System
時間枠:1 week before the study (T0); at week 4 (T1) and at week 8 (T2)
Objective balance performance will be assessed using the Becure Balance System. The system utilizes the Nintendo WiiFit balance board integrated with computer-based software to evaluate static standing balance, center of gravity distribution, and postural oscillations. The validity and reliability of the system have previously been established.
1 week before the study (T0); at week 4 (T1) and at week 8 (T2)

二次結果の測定

結果測定
メジャーの説明
時間枠
Cognitive Assessment
時間枠:1 week before the study (T0); at week 4 (T1) and at week 8 (T2)
The Montreal Cognitive Assessment Scale (MoCA) will be used to assess changes in cognitive levels after the exercise program. The scale is scored between 0 and 30, and includes 6 cognitive functions (memory, visual-spatial skills, executive functions, attention, concentration and working memory tasks, language, and orientation). Higher scores indicate better cognitive performance.
1 week before the study (T0); at week 4 (T1) and at week 8 (T2)
Quality of Life Assessment
時間枠:1 week before the study (T0); at week 4 (T1) and at week 8 (T2)
The Quality of Life Scale in the Elderly (CASP-19) will be used to determine changes in the volunteers' quality of life after the exercise program. CASP-19 consists of 19 items and 4 sub-dimensions as 'Control', 'Autonomy', 'Enjoyment', and 'Self-actualization'. Each item of the scale is rated on a 4-point Likert scale (0-3). Higher scores indicate better perceived quality of life and well-being in older adults.
1 week before the study (T0); at week 4 (T1) and at week 8 (T2)
Assessment of Mobility
時間枠:1 week before the study (T0); at week 4 (T1) and at week 8 (T2)

The Timed Up and Go test (TUG) will be used to assess mobility along with fall risk. TUG correlates well with balance, gait speed, and functional capacity.

In this test, participants are instructed to stand up from a standard chair, walk 3 meters at a comfortable, safe pace, turn around, walk back to the chair, and sit down again.

The total time required to complete the task is recorded in seconds. Shorter completion times indicate better functional mobility and dynamic balance, whereas longer times indicate poorer mobility and increased fall risk.

1 week before the study (T0); at week 4 (T1) and at week 8 (T2)
Upper Extremity Muscle Strength Assessment
時間枠:1 week before the study (T0); at week 4 (T1) and at week 8 (T2)

The Weight Lifting Test (Arm Curl Test) will be used to assess upper extremity muscle strength. Participants perform as many arm curls as possible within 30 seconds while holding a standardized weight [5 lbs (2.3 kg) for women and 8 lbs (3.6 kg) for men].

Higher repetition counts indicate better upper extremity muscle strength.

1 week before the study (T0); at week 4 (T1) and at week 8 (T2)
Upper Extremity Flexibility Assessment
時間枠:1 week before the study (T0); at week 4 (T1) and at week 8 (T2)
Upper extremity flexibility will be assessed using the Back Scratch Test (Apley Scratch Test). The test measures the distance between or the overlap of the middle fingers behind the back. An overlap between the fingers is recorded as a positive value, whereas a gap between the fingers is recorded as a negative value. Higher positive values indicate better upper extremity flexibility.
1 week before the study (T0); at week 4 (T1) and at week 8 (T2)
Lower Extremity Muscle Strength Assessment
時間枠:1 week before the study (T0); at week 4 (T1) and at week 8 (T2)
Lower extremity muscle strength will be assessed using the 30-Second Sit-to-Stand Test. Participants perform as many sit-to-stand repetitions as possible within 30 seconds. Higher repetition counts indicate better lower extremity muscle strength.
1 week before the study (T0); at week 4 (T1) and at week 8 (T2)
Lower Extremity Flexibility Assessment
時間枠:1 week before the study (T0); at week 4 (T1) and at week 8 (T2)
Lower extremity flexibility will be assessed using the Chair Sit-and-Reach Test. The test measures the distance between the fingertips and toes while reaching toward the foot from a seated position. The distance between the fingertips and the toes is measured in centimeters. Reaching beyond the toes is recorded as a positive value, whereas the inability to reach the toes is recorded as a negative value. Higher positive values indicate better lower extremity flexibility.
1 week before the study (T0); at week 4 (T1) and at week 8 (T2)

その他の成果指標

結果測定
メジャーの説明
時間枠
The Mini-Mental State Examination (MMSE)
時間枠:1 week before the study (T0)

The Mini-Mental State Examination (MMSE) will be used to identify the volunteers to be included in the study, as volunteers scoring 24-point or higher on the MMSE will be included in the study.

The MMSE is a 30-point questionnaire commonly used to evaluate cognitive function, including orientation, attention, memory, language, and visuospatial skills. Scores range from 0 to 30, with higher scores indicating better cognitive function.

1 week before the study (T0)

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。

スポンサー

協力者

捜査官

  • スタディディレクター:Pınar Kaya Sarıbaş, Assoc. Prof.、Medipol University
  • 主任研究者:İlkay Tuğçe Köse, M.Sc.、Istanbul Gedik 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 (推定)

2026年6月25日

一次修了 (推定)

2027年6月25日

研究の完了 (推定)

2027年9月30日

試験登録日

最初に提出

2026年5月5日

QC基準を満たした最初の提出物

2026年5月25日

最初の投稿 (実際)

2026年6月1日

学習記録の更新

投稿された最後の更新 (実際)

2026年6月1日

QC基準を満たした最後の更新が送信されました

2026年5月25日

最終確認日

2026年5月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • IGUN-ITKOSE-001

医薬品およびデバイス情報、研究文書

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

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

購読する