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临床试验/CTRI/2024/12/078391
CTRI/2024/12/078391尚未招募不适用

Mobile application for Shoulder rehabilitation

Naveen kumar1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年12月29日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
30
试验地点
1
主要终点
Enhanced functional recovery, including improvements in shoulder function, range of motion,strength, and mobility, as measured by validated

研究概览

简要总结

The mobile application for shoulder rehabilitation aims to enhance the recovery process and outcomes for patients . Through a user-friendly platform, the app guides patients through their rehabilitation exercises, tracks their progress, and educates them about recovery journey. Furthermore, it fosters communication between patients and healthcare providers, facilitating timely support and guidance. Overall, the app seeks to improve patient engagement and adherence to rehabilitation protocols, ultimately leading to better recovery outcomes and overall satisfaction with the treatment process

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patients who needs shoulder rehabilitation Individuals who have access to a smartphone or tablet device with internet connectivity.
  • Participants willing and able to engage in post-operative rehabilitation exercises and activities.
  • Patients with sufficient understanding and proficiency in the language(s) supported by the mobile application.
  • Patients who have completed the immediate post-operative recovery phase and have been cleared by their healthcare provider to begin rehabilitation.

排除标准

  • Individuals with cognitive impairments or mental health conditions that may affect their ability to use the mobile application effectively.
  • Patients with contraindications or complications that require specialized rehabilitation interventions beyond the scope of the mobile application.
  • Participants with severe mobility limitations or comorbidities that may prevent them from safely performing rehabilitation exercises.
  • Patients who are unable or unwilling to provide informed consent for participation in the study.
  • Individuals currently participating in other rehabilitation programs or clinical trials , to avoid confounding variables.

结局指标

主要结局

Enhanced functional recovery, including improvements in shoulder function, range of motion,strength, and mobility, as measured by validated

时间窗: 3 weeks after the start of rehabilitation

clinical scales over the study period.

时间窗: 3 weeks after the start of rehabilitation

次要结局

  • Improved rehabilitation adherence rates assessed through engagement metrics in the mobile application.(Increased patient satisfaction evaluated via standardized satisfaction surveys.)

研究者

发起方
Naveen kumar
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Naveen Kumar

Saveetha medical college and hospital

研究点 (1)

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