Telerehabilitation in Individuals With Chronic Disease

NCT04484389 | Unknown

• 1 other identifier: 015
• Study Type: interventional
• Target: 60
• Locations: 0 countries
• Sites: N/A

Brief Summary

Telerehabilitation applications are a treatment method that uses new technologies. There are examples of doing for many diseases in our country. It is a method used for people living in remote areas and people who cannot complete their treatment in hospitals due to the epidemic. In our study, we will use the telerehabilitation system. In this system, which we will use in people with chronic disease, we aim to see improvement in tests performed in many areas such as physical activity level, respiratory capacity, depression, and anxiety level of patients. In the study to be performed on 60 patients, 30 people will be control and 30 people will be the experimental group. The experimental group will be treated with a video conferencing method, tailor-made exercise program based on the international physical activity questionnaire level for 30 minutes 3 days a week for 6 weeks. The control group will only be informed with the help of a brochure with a standard exercise program. The tests we can use in this experiment are as follows: Barthel daily life activities index, beck depression and anxiety scale, ferrans power quality of life index, Charlson comorbidity index, environmental measurements, waist/hip ratio, fatigue severity scale, international physical activity questionnaire. Tests specific to chronic diseases will be applied to patient one to one.

Conditions

Telerehabilitation

Keywords

Chronic Disease; Exercises; Social Isolation

Outcome Measures

Primary Outcomes (1)

• Beck Depression Inventory

  The Beck Depression Inventory is a 21-item, self-report rating inventory that measures characteristic attitudes and symptoms of depression. Beck Depression Inventory is a 21-question multiple-choice self-report inventory The Beck Depression Inventory takes approximately 10 minutes to complete. The minimum score that can be obtained from the scale is 0 and the maximum score is 63 . Higher total scores indicate more severe depressive symptoms.

  2 weeks

Secondary Outcomes (1)

• Charlson Comorbidity Index

  2 weeks

Other Outcomes (7)

• The Beck Anxiety Inventory

  2 weeks

• MODIFIED FATIGUE IMPACT SCALE

  2 weeks

• The Fatigue Severity Scale

  2 weeks

Study Arms (2)

Study Group

EXPERIMENTAL

Individual exercises will be applied to individuals with Chronic disease.

Other: Telerehabilitation

Control Group

ACTIVE COMPARATOR

Group to be given an exercise brochure

Other: Exercise brochure

Interventions

Telerehabilitation OTHER

Exercise protocol according to Ipaq will be prepared for 30 patients with chronic disease . Exercise protocol; warm-up exercises include, stretching exercises, postural exercises, aerobic exercise and cooling exercises. People will practice the exercises 3 days a week for 6 weeks. People will need to reserve 30 minutes a day for this study.

Study Group

Exercise brochure OTHER

General exercise protocol will be prepared and given to the control group as a brochure

Control Group

Eligibility Criteria

• Age: 18 Years - 79 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Having a chronic disease
• To be able to communicate verbally
• Being in a stable period in terms of disease
• At least 3 months for the disease to be chronic
• Regulated hypertension
• Diabetes patients should have them blood sugar under 200 during therapy

You may not qualify if:

• Dementia
• Being a cancer patient receiving chemotherapy
• Epilepsy and a history of seizures
• Patient who has recently undergone surgery
• Pregnancy
• Delirium
• Bedridden

Sponsors & Collaborators

• Istinye University: lead

MeSH Terms

Conditions

Chronic Disease; Motor Activity; Social Isolation

Interventions

Telerehabilitation

Condition Hierarchy (Ancestors)

Disease Attributes; Pathologic Processes; Pathological Conditions, Signs and Symptoms; Behavior; Social Behavior

Intervention Hierarchy (Ancestors)

Rehabilitation; Aftercare; Continuity of Patient Care; Patient Care; Therapeutics; Health Services; Health Care Facilities Workforce and Services; Telemedicine; Delivery of Health Care; Patient Care Management; Health Services Administration

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: PARTICIPANT
• Masking Details: Single
• Purpose: PREVENTION
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Investigator

Study Record Dates

• First Submitted: July 20, 2020
• First Posted: July 23, 2020
• Study Start: August 15, 2020
• Primary Completion: August 15, 2021
• Study Completion: August 31, 2021
• Last Updated: July 30, 2020

Record last verified: 2020-07

Data Sharing

• IPD Sharing: Will not share