The Effects of Telerehabilitation And Chair-based Yoga In The Elderly

October 26, 2022 updated by: Sevval Kadriye Bakir

The Effects of Chair-Based Yoga With Telerehabilitation on Function and Quality of Life in Elderly Individuals

The aim of the study is to investigate the effects of chair-based yoga with rehabilitation on quality of life is affected in elderly people. Depending on the changes in the body as a result of aging, people's quality of life is affected. In order to increase or protect the quality of life in elderly people, telerehabilitation practices are emphasized. Telerehabilitation is a promising system for the elderly thanks to its advantages.

As a practice, chair-based yoga, a modified form of yoga, was preferred. Chair-based yoga makes yoga more doable and safe for older people. Chair-based yoga with telerehabilitation was performed with the participants. Pain level, sleep status, functional capacity, quality of life, mental health and depression were followed by evaluations at the beginning and end of the process.

Study Overview

Study Type

Interventional

Enrollment (Actual)

32

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 Locations

    • Balıkesir
      • Istanbul, Balıkesir, Turkey, 34010
        • Istinye University Topkapi Campus

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

65 years and older (Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • 65 years and over,
  • Having a Standardized Mini Mental Test Score of 24 and above,
  • physically active (self-sustaining),

Exclusion Criteria:

  • severe cardiopathy,
  • uncontrolled hypertension,
  • mental disorder,
  • Presence of any health condition that may prevent functional autonomy test such as hearing and vision,
  • have mental disorders and dementia,
  • people with any unstable medical condition

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: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Study Group
chair-based yoga program with tele-rehabilitation was applied to elderly people.
Chair-based yoga with telerehabilitation was applied to the study group for 45 minutes a day, 2 days a week, for 6 weeks.
Active Comparator: Control Group
1 session of training was given on the effect of physical activity and exercise on function and quality of life.
A one-session training was provided on the effects of exercise on quality of life.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Senior Fitness Test (SFT)
Time Frame: 6 weeks
It is another test protocol in which the physical fitness of elderly people is evaluated with a few test parameters. SFT Test Protocol; It consisted of 6 stations including chair sit-stand, weight lifting, chair sit-down, 2-minute stepping, 8-step up-go and back scratching tests.
6 weeks
Nottingham Health Profile (NHP)
Time Frame: 6 weeks
It is a general patient-reported outcome measure intended to measure subjective health status. It is a questionnaire designed to measure a patient's views on his or her health status in various fields. It can be completed in 5 minutes. NHP consists of two parts.
6 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Charlson Comorbidity Index
Time Frame: 6 weeks
Scaling that can be applied by quantifying comorbidities and examining their effects on prognosis in clinical trials, with the informant or by obtaining information from medical records. 19 disease states are evaluated.
6 weeks
Barthel Index for Activities of Daily Living
Time Frame: 6 weeks
Scaling with the informant to assess the physical adequacy of geriatric subjects and their independence in basic activities of daily living. 10 activities of daily living are evaluated. The Bartel index (BI) is a widely used scale in functional disability.
6 weeks
Mini Mental State Assessment
Time Frame: 6 weeks
Screening test in which cognitive functions are evaluated globally. With the standardized mini mental test, the patient is evaluated under 5 main headings.
6 weeks
Yesavage Geriatric Depression Scale
Time Frame: 6 weeks
Scaling applied to evaluate geriatric cases in terms of depressive mood. General mood characteristics such as attentional state, decision-making process, and perspective on the future are questioned.
6 weeks
Tinetti Balance and Gait Test
Time Frame: 6 weeks
It is a scaling applied in the presence of an observer in order to evaluate the walking and balance abilities of the person. It consists of 16 questions. TDYD evaluates balance ability and gait under 2 main headings.
6 weeks
Clinical Frailty Scale
Time Frame: 6 weeks
It is a scaling that can be done with the case itself or the caregiver in order to evaluate the cases in terms of fragility with clinical findings. It consists of 9 questions.
6 weeks
Pittsburgh Sleep Quality
Time Frame: 6 weeks
It is a scale that evaluates sleep quality with a total of 19 questions under 7 main headings. The 18 scored questions of the scale consist of 7 components. Subjective Sleep Quality, Sleep Latency, Sleep Duration, Habitual Sleep Efficiency, Sleep Disorder, Sleeping Drug Use, and Daytime Dysfunction. Each component is evaluated over 0-3 points.
6 weeks
Mc Gill Pain Questionnaire
Time Frame: 6 weeks
It consists of four parts. In the first part, the patient is asked to mark the location of the pain on the body chart. Part Two: In this part, there are 20 sets of words that examine pain in terms of sensory, perceptual and evaluation. The patient is told to choose the word set that fits his pain and to mark the word that fits his pain in the chosen set. In the third part, the relationship of pain with time takes place. There are word groups to determine the continuity of pain, its frequency, and factors that increase/reduce pain. In the fourth part, five word groups ranging from "mild" pain to "unbearable" pain to determine the severity of pain; In addition, six questions were included to determine the severity of pain that the patient can accept or experience without discomfort, which is also defined as "experienceable=target pain".
6 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Şevval Bakır, sevval.bak19@gmail.com
  • Study Director: Gül D Yelvar, guldenizy@yahoo.com

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)

December 1, 2020

Primary Completion (Actual)

March 1, 2021

Study Completion (Actual)

March 1, 2022

Study Registration Dates

First Submitted

October 26, 2022

First Submitted That Met QC Criteria

October 26, 2022

First Posted (Actual)

October 28, 2022

Study Record Updates

Last Update Posted (Actual)

October 28, 2022

Last Update Submitted That Met QC Criteria

October 26, 2022

Last Verified

October 1, 2022

More Information

Terms related to this study

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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