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Improving Posture Parameters of Primary Care Providers to Individuals With Disabilities

I

Istanbul Medeniyet University

Status

Enrolling

Conditions

Physical Disability

Treatments

Other: exercises

Study type

Interventional

Funder types

Other

Identifiers

NCT05909449
2023-9169

Details and patient eligibility

About

The aim of this research is to create and implement an exercise program so that primary caregivers can have the correct posture and improve health-related physical fitness parameters.

Full description

It is planned to include at least 40 volunteers between the ages of 18-65 who meet the inclusion criteria and provide primary care services to individuals with disabilities who attend Sportive Skills and Coordination Training Centers operating in the provinces of Istanbul and Gaziantep within the body of the Foundation for the Physically Disabled. Musculoskeletal complaints of caregivers related to the care process (neck pain, low back pain and upper extremity pain), physical fitness parameters (functional capacity and shortness-flexibility, balance and footpad pressure distribution), the effects of the caregiving process on the caregiver and mental well-being will be evaluated.

After the first evaluation, the participants will be given an informative training seminar on the effects of exercise on healthy life and the regulation of ergonomics in our behaviors. After the seminar, participants will be included in a structured home exercise program. The home exercise program prepared by the research team and recorded on video will be delivered to the participants. The exercise program will be continued for 6 weeks, 3 days a week. The exercise program will be prepared weekly to advance to the next level. Exercise compliance and attendance will be monitored weekly by the researchers. Evaluations will be repeated at the end of the 6-week exercise program.

Establishment of an exercise program: In the light of the data obtained as a result of the evaluations, an individual-specific exercise program will be created. The exercises will be taught one-on-one to the participants. With the exercise video prepared by the project team and sent to the patients, the participants will be prevented from forgetting the exercises and they will be stimulated to do the exercises correctly. The content of the exercise program will include exercises that include aerobic, strengthening and flexibility components. The exercise program will take approximately 30-45 minutes.

Enrollment

40 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Individuals between the ages of 18-65
  • To give primary care to a person with a physical disability
  • Being caring for at least 6 months
  • Voluntarily performing care
  • Being able to understand and read Turkish as a language
  • To have sufficient cognitive level to answer the scale questions with the basic interview
  • Volunteer to participate in and maintain an exercise program
  • Regularly participating in the evaluation and exercise program defined during the project process

Exclusion criteria

  • Caring for a paid job other than voluntarily
  • Encountering a disease related to the caregiver during the working process
  • Having any known musculoskeletal disease
  • Having a known spinal problem such as scoliosis, kyphosis, kyphoscoliosis
  • Having undergone surgery affecting the musculoskeletal system in the last 1 month
  • History of uncontrollable arrhythmia and/or hypertension
  • Having any neurological, cardiovascular, respiratory, orthopedic and metabolic disease that will prevent participation in the exercise program
  • Being pregnant for female individuals

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

40 participants in 1 patient group

research group
Experimental group
Description:
provide primary care services to individuals with physical disabilities
Treatment:
Other: exercises

Trial contacts and locations

1

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Central trial contact

GÜLSER CİNBAZ

Data sourced from clinicaltrials.gov

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