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临床试验/NCT03729466
NCT03729466Unknown不适用

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

Eastern Mediterranean University2 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2018年10月4日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
70
试验地点
2
主要终点
Fatigue severity scale

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 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)

排除标准

  • 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

研究组 & 干预措施

Control group

No Intervention

There will be no intervention for 8 weeks

Intervention group

Experimental

clinical pilates will be given to the intervention group for 8 weeks

干预措施: clinical pilates (Other)

结局指标

主要结局

Fatigue severity scale

时间窗: up to 8 weeks

The items are scored on a 7 point scale with 1 = strongly disagree and 7= strongly agree

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Yazgı Şentürk

Principal Investigator Yazgı Şentürk

Eastern Mediterranean University

研究点 (2)

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