NCT06548880

Brief Summary

The aim of this study is to investigate the effectiveness of online exercise training in geriatric population whose daily life activity level decreased during COVID-19 pandemic. The main questions it aims to answer are:

  • Does online exercise training improve quality of life in the geriatric population whose daily life activity levels have decreased during the COVID-19 pandemic?
  • Does online exercise training improve sleep quality in the geriatric population whose daily life activity levels have decreased during the COVID-19 pandemic?
  • Does online exercise training affect depression status in the geriatric population whose daily life activity levels have decreased during the COVID-19 pandemic?
  • Does online exercise training reduce the risk of falls by improving balance and functional independence in geriatric population whose daily life activity levels have decreased during the COVID-19 pandemic?
  • Does online exercise training improve posture in geriatric population whose daily life activity levels have decreased during the COVID-19 pandemic? Research data were collected by Sociodemographic Information Form, 36-Item Short Form Survey, The Pittsburgh Sleep Quality Index, Geriatric Depression Scale, Timed Up \& Go Test, and New York Posture Rating Chart. While no application was given to the control group, study group has received an online exercise training with a structured exercise program including range of motion, stretching, and, to train full body, low intensity aerobic exercises, once a week for 10 weeks, each lasting 60 minutes.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Apr 2022

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2022

Completed
1.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 31, 2023

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 31, 2023

Completed
11 months until next milestone

First Submitted

Initial submission to the registry

August 8, 2024

Completed
4 days until next milestone

First Posted

Study publicly available on registry

August 12, 2024

Completed
Last Updated

January 14, 2025

Status Verified

August 1, 2024

Enrollment Period

1.2 years

First QC Date

August 8, 2024

Last Update Submit

January 10, 2025

Conditions

Keywords

COVID-19activities of daily livinggeriatricstelerehabilitation

Outcome Measures

Primary Outcomes (2)

  • balance

    To determine fall risk and measure the progress of balance, sit to stand and walking, Timed-Up and Go Test was used. This is a simple screening test that is a sensitive and specific measure of probability for falls among older adults. An older adult who takes ≥12 seconds to complete the test is at risk for falling. The results of the Timed-Up and Go Test were obtained in seconds. This primary outcome was evaluated by interpreting these results.

    This outcome was evaluated twice, before starting the exercise program and after completing the exercise program.

  • mobility

    To determine fall risk and measure the progress of balance, sit to stand and walking, Timed-Up and Go Test was used. This is a simple screening test that is a sensitive and specific measure of probability for falls among older adults. An older adult who takes ≥12 seconds to complete the test is at risk for falling. The results of the Timed-Up and Go Test were obtained in seconds. This primary outcome was evaluated by interpreting these results.

    This outcome was evaluated twice, before starting the exercise program and after completing the exercise program.

Secondary Outcomes (4)

  • sleep quality

    This outcome was evaluated twice, before starting the exercise program and after completing the exercise program.

  • depression status

    This outcome was evaluated twice, before starting the exercise program and after completing the exercise program.

  • posture

    This outcome was evaluated twice, before starting the exercise program and after completing the exercise program.

  • QoL

    This outcome was evaluated twice, before starting the exercise program and after completing the exercise program.

Study Arms (2)

Study group

EXPERIMENTAL

Participants in the study group have received an online exercise training with a structured exercise program including range of motion, stretching, and, to train full body, low intensity aerobic exercises, once a week for 10 weeks, each lasting 60 minutes.

Other: Structured exercise program

Control group

NO INTERVENTION

Participants in the control group were asked to maintain their daily physical activity routine.

Interventions

The intervention applied in this research has an online exercise training conducting with a structured exercise program including different types of exercise which are range of motion, stretching and low intensity aerobic exercises. The exercise program continued with sessions each lasting 60 minutes, once a week for 10 weeks.

Study group

Eligibility Criteria

Age65 Years - 95 Years
Sexall
Healthy VolunteersYes
Age GroupsOlder Adult (65+)

You may qualify if:

  • Volunteering to participate in the study
  • Being over 65 years old

You may not qualify if:

  • Having mental retardation at a level that prevents communication
  • Having an uncontrollable heart and hypertension problem
  • Being receiving medical treatment or rehabilitation for balance that may affect the balance level
  • Having osteoporosis at a level where exercise can be considered risky
  • Having a health problem where exercise is considered contraindicated

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Medipol University

Istanbul, 34000, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Sedentary BehaviorCOVID-19

Condition Hierarchy (Ancestors)

BehaviorPneumonia, ViralPneumoniaRespiratory Tract InfectionsInfectionsVirus DiseasesCoronavirus InfectionsCoronaviridae InfectionsNidovirales InfectionsRNA Virus InfectionsLung DiseasesRespiratory Tract Diseases

Study Officials

  • Gönül ERTUNÇ GÜLÇELİK, Ph.D.

    Kocaeli University

    STUDY CHAIR
  • Sıla YILMAZ, M.Sc.

    Medipol University

    STUDY DIRECTOR
  • Fatma Nur DÜLGER, Miss

    Medipol University

    PRINCIPAL INVESTIGATOR
  • Elvan EKİNCİ, Miss

    İstanbul Gedik University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: 10 participants were included in the study group, and 10 participants were included in the control group.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer

Study Record Dates

First Submitted

August 8, 2024

First Posted

August 12, 2024

Study Start

April 1, 2022

Primary Completion

May 31, 2023

Study Completion

August 31, 2023

Last Updated

January 14, 2025

Record last verified: 2024-08

Locations