The Effects of Somatic-Based Chair Exercises in the Elderly

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age65+
SponsorIstanbul Gedik University

About this trial

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?

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

65 years of age or older

To be volunteered to participate

To be able to speak and understand Turkish at a good level

Disqualifiers

Scoring <24 on the Mini-Mental State Examination

Any neurological or orthopedic problem that would prevent the implementation of assessment and exercise methods

Trial design

Design model

Parallel

Treatments tested in this trial

  • Somatic-Based Chair Exercises

    Other intervention

    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.

  • Conventional Exercise Group

    Other intervention

    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.

Treatment groups

70 Participants
are divided into 2 treatment groups
Group A: Somatic-based Chair Exercise GroupExperimental treatment 1 intervention
Group B: Conventional Exercise GroupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Pain Assessment

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).

Time frame
1 week before the study (T0); at week 4 (T1) and at week 8 (T2)
2

Balance Ability Assessment

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.

Time frame
1 week before the study (T0); at week 4 (T1) and at week 8 (T2)
3

Objective Balance Assessment via Becure Balance System

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.

Time frame
1 week before the study (T0); at week 4 (T1) and at week 8 (T2)

Secondary outcomes

1

Cognitive Assessment

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.

Time frame
1 week before the study (T0); at week 4 (T1) and at week 8 (T2)
2

Quality of Life Assessment

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.

Time frame
1 week before the study (T0); at week 4 (T1) and at week 8 (T2)
3

Assessment of Mobility

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.

Time frame
1 week before the study (T0); at week 4 (T1) and at week 8 (T2)
4

Upper Extremity Muscle Strength Assessment

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.

Time frame
1 week before the study (T0); at week 4 (T1) and at week 8 (T2)

Other outcomes

1

The Mini-Mental State Examination (MMSE)

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.

Time frame
1 week before the study (T0)

Locations

This trial has no locations.

Sponsors and contacts

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Istanbul Gedik University

Lead sponsor

Medipol University

Sponsor institution

Medipol University

Collaborator

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