Investigation of the Effects of Clinical Pilates Exercises on Primary Caregivers of Special Needs Children

Sedentary Lifestyle Clinical Trial

Official title:

Investigation of the Effects of Clinical Pilates Exercises on Primary Caregivers of Special Needs Children: Randomized Comparative Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03729466
• Other study ID #: ETK00-2018-0154
• Status: Recruiting
• Phase: N/A
• Start date: October 4, 2018
• Est. completion date: December 5, 2018

Study information

• Verified date: November 2018
• Source: Eastern Mediterranean University
• Contact: Yazgi Sentürk
• Phone: 05428862868
• Email: yazgisntrk[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The aim of this research is to investigate the effectiveness of clinical Pilates exercises applied to primary caregivers of children with special needs, flexibility, muscle strength, endurance, cardiovascular endurance, fatigue, coping attitudes and quality of life, depression and anxiety.

Description:

Individuals participating in the study will be randomly divided into two groups through the randomized allocation software program. The first group will be given Clinical Pilates exercise training, while the second group will be considered as the control group. The exercises will be applied to the group attending the Clinical Pilates exercise training for 45-60 minutes, twice a week for a total of 8 weeks. Each movement will consist of one set and 10 repetitions. In the Clinical Pilates program, equipment and exercises will be gradually increased. Equipment to be used throughout the Clinical Pilates program; Pilates cushion, Elastic resistant band (red, green, blue), Exercise ball (65 cm) In the Clinical Pilates group, the training session will start with the warm-up program, core stabilization training, clinical Pilates exercises will be applied to increase the postural smoothness and strength, and the exercise session will be terminated with the cooling period. The clinical Pilates group will be given 5 key elements of clinical Pilates (Respiratory-Centre focus- Chest placement - Shoulder placement - Head-neck placement) will be explained. No exercise program will be applied to the control group for 8 weeks. A sufficient number of trials will be conducted to enable participants to adapt to the evaluation and treatment. The evaluations will be done as pre-test and post-test for both groups and then the groups will be compared. Individuals who have agreed to participate in the study and have signed the information consent form will be included.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 70
• Est. completion date: December 5, 2018
• Est. primary completion date: October 25, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

• Caring for children over 3 years of age=1 with special needs,

• Caring for the child for at least 6 months, with or without blood connection (mother, father, nan, aunt, sibling, carer, etc.)

• Being between the ages of 18-55,

• Has not had regular exercise in the last 6 months (3 days a week, more than 20 minutes)

Exclusion Criteria:

• Have serious orthopaedic, neurological, rheumatologic and psychiatric problems that may prevent clinical Pilates exercises.

• Pregnancy

• Has had a traumatic injury or surgery in the last 6 months

Related Conditions & MeSH terms

• Sedentary Lifestyle

Intervention

Other:
• clinical pilates
The intervention group will be performed in clinical pilates 45 to 60 minutes twice a week for 8 weeks.

Locations

Country	Name	City	State
Cyprus	Eastern Mediterrean Universty	Famagusta

Sponsors (1)

Lead Sponsor	Collaborator
Eastern Mediterranean University

Country where clinical trial is conducted

Cyprus, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Fatigue severity scale	The items are scored on a 7 point scale with 1 = strongly disagree and 7= strongly agree	up to 8 weeks