Comparative Effects of Sensory Integration Therapy and Balance Board Training in Community Dwelling Older Adults

June 24, 2024 updated by: Riphah International University

Comparative Effects of Sensory Integration Therapy and Balance Board Training on Balance, Postural Stability, Functional Mobility and Risk of Fall in Community Dwelling Older Adults

Balance plays a significant role in stability and walking and it's essential for improving the quality of life and functional autonomy while reducing the risk of falling. This research intends to shed light on the advantages of sensory integration therapy and balance board training because it is important to addressing the issues related to ageing and their possible effects.

Study Overview

Status

Recruiting

Conditions

Detailed Description

Previously the study was conducted to determine how sensory integration training affected older persons (aged 50 to 80) in terms of their ability to balance. Twelve healthy volunteers and eight people who had suffered a chronic stroke were included in this study. The participants were trained for six weeks. During standing and dynamic base-of-support exercises, repeated sensory training targeted visual and somatosensory inputs. The balance error scoring system, was used to evaluate standing balance both before and after training. With the exception of the most difficult condition (the single leg stand on a foam surface), there were no appreciable declines (improvements in balance) between pre and post-test for the healthy individuals. It was noted that the stroke participants' ability for balance had increased.

The study conducted in 2021 aimed at the comparison between the effects of virtual reality training (VRT) and conventional balance training (CBT) on the balance of the elderly. 36 elderly who are living in nursing homes were randomly divided into three groups: virtual reality training, conventional balance training and control group. Each group participated in a 60 min session, 3 times per week for 9 weeks. To assess the balance, the balance tests were used on single-leg stance (STS) with open and closed eyes, functional reach test (FRT), timed up and go test (TUG) and Fullerton advance balance scale (FABS). After the intervention the results showed that neither VRT nor CBT training method superior to other.

In 2020, a study was conducted to determine how combined strength and balance training affected the measurements of muscular strength and balance in older women who had previously had falls. Twenty-seven senior ladies were divided into two groups at random: the intervention group (IG, n = 12) and the control group (CG, n = 15). The IG underwent eight weeks of combined strength and balance training, consisting of three sessions per week with force plate visual biofeedback. .. At a rehabilitation facility, the CG got physical treatment and gait training. balance, and muscle strength (assessed by the sit-to-stand test, weight-bearing squat, which calculates the proportion of body mass supported by each leg at various knee flexions [0°, 30°, 60°, and 90°). The modified clinical test of sensory interaction was utilized for balance assessments. This study shows that combined strength and balance training reduced sway oscillation in the IG and enhanced the percentage distribution of body weight between the legs.

Previously a study aimed to assess the efficacy of long term balance training with and without sensory augmentation among community dwelling healthy older adults. Twelve participants were randomly assigned into two groups. The experimental group received vibrotactile sensory augmentation through the smart phone balance trainers. While the control group performed exercises without sensory augmentation. Balance performance was assessed by using (activity balance confidence scale, sensory organization test, mini balance evaluation, Functional reach test, gait speed test, time up and go). After training the experimental group had significantly greater impairments in sensory organization test and mini balance evaluation systems test score than control group.

The study was conducted aimed to investigate the feasibility of a home based Wi balance training with mobile older stroke survivors. 14 persons participated in the study and were randomized to the training group (n=6) and the conventional balance training group (n=8). To get information about individual balance deficits that berg balance scale and dynamic gait index, ABC scale, timed up and go test (TUG) and a posturographic measurement were conducted. The results showed that unsupervised use of Wii balance board in the home environment seems possible and adequate for older stroke survivors with low functional limitation.

The study was to assess to which extent two similar skiing games challenge balance, as reflected in center of mass (COM) movements relative to their functional limits of stability (FLOS). Thirty young and elderly participants performed two skiing games, one on the Wii balance board (wiiski), which uses a force plate and one with the Kinect sensor (kinski), which performs motion tracking. During gameplay, kinematics were captured using seven opto electronical cameras. Subjects showed significantly larger maximal %FLOS displacement during the kinski game than during the Wiiski game. Furthermore, maximal COM displacement and COM speed in kinski remained similar or increased over trials, whereas for Wiiski it decreased.

Though, exercise is considered significant for older adults, most of the available literature and publications focuses on individual exercise interventions rather than directly comparing them. Thus, up to the author's knowledge, no studies have been found to compare how balance board training and sensory integration treatment affects functional mobility, postural stability, balance, and fall risk. Moreover, the literature on the relationship between improving balance and sensory integration is quite thin. Among latest researches, only fewer provide thorough procedures for sensory integration treatment and balance board training. Therefore, Present study aims to bridge this gap by optimizing exercise strategies and providing the evidence-based recommendations tailored to the unique needs of older adults.

Study Type

Interventional

Enrollment (Estimated)

58

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Punjab
      • Lahore, Punjab, Pakistan, 54000
        • Recruiting
        • Al-Shifa Malik Hospital
        • Contact:
        • Principal Investigator:
          • Mahrukh Yaseen, DPT
      • Lahore, Punjab, Pakistan, 54000
        • Recruiting
        • Gosha e Shifa Hosital
        • Contact:
        • Principal Investigator:
          • Mahrukh Yaseen, DPT

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Should be living independently (FIM 108-126).
  • No history of lower limb injury in the 1 year prior to the study.
  • Individuals with MMSE score greater than or equal to 24.
  • Individuals with BBS score 41-56.

Exclusion Criteria:

  • Individuals with recent cardiac or neurological changes in medical status.
  • Individuals with recent surgical procedures within the last 6 months will not include in the study.
  • Individuals with the presence of inner ear problems, dizziness, long-term medication.
  • A history of injury within 1 year before the study.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Sensory Integration Therapy
Sensory integration therapy in older adults focuses on optimizing sensory processing to enhance overall function and well-being. It aims to improve sensory perception, coordination, and integration, which are essential for maintaining balance and mobility
This group will receive sensory integration therapy for 30 minutes along with routine physical therapy treatment (warm up exercises and Stretching exercises (hamstrings, quadriceps, and calf muscles) for 15 minutes per session for 3 days a week for 8 week.
Active Comparator: Balance Board Training
Balance board training in older adults is a targeted approach aimed at enhancing stability and reducing fall risk. Utilizing specialized boards, it challenges balance control and proprioception, crucial for maintaining equilibrium. Through regular practice, older adults can improve muscle strength, coordination, and confidence in weight-bearing activities
This group will receive balance board training for 30 minutes along with routine physical therapy treatment (warm up exercises and Stretching exercises (hamstrings, quadriceps, and calf muscles) for 15 minutes per session for 3 days a week.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Berg Balance Scale
Time Frame: 8th week
Berg balance scale is used to find and access the balance issues. This scale consists of 14 task which related to everyday life. Each function rates from 0 (worst) to 4 (best) along a dependence and independence sequence. In this test, we gradually reduce the base of support from sitting and standing to single-leg stance, assess a subject's capacity to sustain positions or movements of increasing difficulty. One's ability to change position is also evaluated
8th week

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Time up and go test
Time Frame: 8th week
The TUG test measures the time, in seconds, taken by an individual to stand up from a standard arm chair, walk at their standard pace a distance of 3 meters, turn, walk back to the chair, and sit down. The TUG is widely used because it is reliable and it tests several important balance and mobility skills, including, sit-to-stand transitions, turning, and gait. Time less than 13.5 seconds indicate good mobility.
8th week
Fall risk assessment tool
Time Frame: 8th week
The Johns Hopkins Fall Risk Assessment Tool (JHFRAT) is a tool that makes possible to implement a multi-factorial assessment of the risk of falling in a simple way, which requires an average of 5 min for its completion. The maximum score for this tool is 20. Score of 16-20 indicate high risk of fall, while the score between 5-10 indicate low risk of fall.
8th week
Functional Reach Test
Time Frame: 8th week

Functional reach test is designed to assess the postural stability. During the test, the person stands next to a wall with their arm raised to 90 degrees. They then reach forward as far as possible without taking a step, while maintaining their balance. The distance reached is measured from the starting position to the fingertips at maximum reach.

A score of 6 or less indicate poor postural stability thereby increasing risk of fall.

A score greater than 10 indicates good postural stability and minimum risk of fall

8th week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Hira Jabeen, Riphah International University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 1, 2024

Primary Completion (Estimated)

August 30, 2024

Study Completion (Estimated)

August 30, 2024

Study Registration Dates

First Submitted

June 11, 2024

First Submitted That Met QC Criteria

June 24, 2024

First Posted (Actual)

June 26, 2024

Study Record Updates

Last Update Posted (Actual)

June 26, 2024

Last Update Submitted That Met QC Criteria

June 24, 2024

Last Verified

June 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • REC/RCR & AHS/23/0299

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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