Remote Exercise Programs and Preventive Training in Asymptomatic Individuals

NCT ID: NCT04704570

Last Updated: 2023-05-31

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

54 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-04-14

Study Completion Date

2023-03-01

Brief Summary

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In recent years, it has been emphasized that preventive approaches are a less costly and more effective way to treat a pathology. Primary preventive approaches should become widespread, especially in problems with changeable risk factors such as spine health. Various preventive approaches and exercise training seem to be an effective way to prevent the development of back and neck pain. Again, in recent years, the pandemic process has increased the interest and need for tele-rehabilitation. As a result, scientific research results on tele-rehabilitation are needed as a necessity to adapt to the Covid-19 epidemic and the globalizing world. The aim of the thesis study planned in this context is to investigate the effectiveness of remote exercise applications on lumbar and cervical region muscle architecture and functionality in asymptomatic individuals.Another aim of this study is to investigate the remote applicability of functional level, quality of life, kinesophobia and cognitive assessment.

Detailed Description

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Conditions

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Healthy People

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Investigators

Study Groups

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Treatment Group

Remotely Exercises 3 times a week, 8 weeks remotely (with video) spinal stabilization exercises

Group Type EXPERIMENTAL

Exercise

Intervention Type OTHER

Spinal stabilization exercise

Control Group

Face to Face Exercises 3 times a week, 8 weeks face to face (in clinic) spinal stabilization exercises

Group Type OTHER

Exercise

Intervention Type OTHER

Spinal stabilization exercise

Remotely assessment Group-Face to Face Assessment Group

First, a remote evaluation and then a face to face evaluation will be made.

Group Type OTHER

Remotely and face to face evaluation of Functional Capacity Level

Intervention Type OTHER

Quality of life assessment (SF-36), and cognitive assessment ((Montreal Cognitive Assessment Scale (MOCA)) will be administered face to face. Functional capacity assessment tests will be administered both face-to-face and remotely. All participants will be administered both remotely and face-to-face. The order of the remote and face-to-face evaluations will be determined by the closed envelope randomization method. The remote evaluation will be done by video interview method under the direction of the researcher. During the remote evaluation, the necessary equipment for the participant will be prepared in the unit in advance. There will be a 10-30 minute rest interval between each evaluation.This application will only be applied at the beginning of the exercise program.After the 8-week program, only face-to-face evaluation will be made.

Face to Face Assessment Group-Remotely assessment Group

First, a facet o face evaluation and then a remote evaluation will be made.

Group Type OTHER

Remotely and face to face evaluation of Functional Capacity Level

Intervention Type OTHER

Quality of life assessment (SF-36), and cognitive assessment ((Montreal Cognitive Assessment Scale (MOCA)) will be administered face to face. Functional capacity assessment tests will be administered both face-to-face and remotely. All participants will be administered both remotely and face-to-face. The order of the remote and face-to-face evaluations will be determined by the closed envelope randomization method. The remote evaluation will be done by video interview method under the direction of the researcher. During the remote evaluation, the necessary equipment for the participant will be prepared in the unit in advance. There will be a 10-30 minute rest interval between each evaluation.This application will only be applied at the beginning of the exercise program.After the 8-week program, only face-to-face evaluation will be made.

Interventions

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Exercise

Spinal stabilization exercise

Intervention Type OTHER

Remotely and face to face evaluation of Functional Capacity Level

Quality of life assessment (SF-36), and cognitive assessment ((Montreal Cognitive Assessment Scale (MOCA)) will be administered face to face. Functional capacity assessment tests will be administered both face-to-face and remotely. All participants will be administered both remotely and face-to-face. The order of the remote and face-to-face evaluations will be determined by the closed envelope randomization method. The remote evaluation will be done by video interview method under the direction of the researcher. During the remote evaluation, the necessary equipment for the participant will be prepared in the unit in advance. There will be a 10-30 minute rest interval between each evaluation.This application will only be applied at the beginning of the exercise program.After the 8-week program, only face-to-face evaluation will be made.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Have not experienced back and neck pain for at least 3 months,
* Between the ages of 18-55,
* Literate,
* Individuals who are capable of understanding exercises (Montreal Cognitive Assessment Scale (MOCA) (19) total score\> 21) will be included in the study.

Exclusion Criteria

* Having been diagnosed with cervical or lumbar region pathologies,
* Cervical radiculopathy, thoracic outlet syndrome,
* Malignant condition,
* Have systemic diseases such as neurological, psychological, cardiovascular, rheumatology and loss of function due to these diseases,
* Previous surgery history in the spine and upper extremity, including the cervical and lumbar region,
* Fracture in the spine and upper extremity, including the cervical and lumbar region, with an inflammatory history,
* Acute infection,
* Continuing another rehabilitation program,
* Individuals who do not agree to participate in the study and do not give written consent will be excluded from the study.
Minimum Eligible Age

18 Years

Maximum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Hacettepe University

OTHER

Sponsor Role lead

Responsible Party

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Yasemin Özel Aslıyüce

Research Assistant, Physiotherapist

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Yasemin Özel Aslıyüce

Ankara, Sıhhiye, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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KA-20110

Identifier Type: -

Identifier Source: org_study_id

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