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临床试验/NCT06874582
NCT06874582已完成不适用

EVALUATION of QUALITY of LIFE, PSYCHOSOCIAL ADAPTATION, and FUNCTIONALITY in SILICONE PROSTHESIS USERS

Medipol University1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2021年10月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
32
试验地点
1
主要终点
Nottingham Health Profile (NHP)

研究概览

简要总结

Objective: This study aimed to evaluate the psychosocial adaptation, functional capacity, and quality of life of individuals who underwent partial hand or foot amputations after using silicone hand and foot prostheses.

Materials and Methods: The study included 32 patients. Demographic and clinical characteristics of the participants were recorded. Participants were divided into two groups as silicone hand or foot prosthesis users. The Visual Analog Scale (VAS) was used to assess pain levels before and after prosthesis use, the Trinity Amputation and Prosthesis Experience Scales (TAPES) were applied to evaluate functional capacity, and the Nottingham Health Profile (NHP) was used to assess quality of life.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Hand and foot amputation.
  • •Aged between 18 and 60 years
  • •Active employee
  • •Able to walk, co-operate, move actively with hands
  • •Who have been using prosthesis for at least 1 year and have good stump-socket compatibility,
  • •Literate individuals were determined on a voluntary basis.

排除标准

  • •Multiple amputations
  • •Severe neurological or traumatic findings
  • •Individuals with severe deformity or posture disorder that may lead to loss of gait, balance or function.
  • •With limitation of movement in the upper extremities

研究组 & 干预措施

silicone hand or finger prosthesis users

Active Comparator

The first arm of our study consisted of participants with partial or finger amputation and silicone hand-finger prosthesis.

干预措施: silicone hand or finger prosthesis (Device)

silicone foot or toe prostheses users

Active Comparator

The second arm of our study consisted of participants with partial or finger amputation and silicone foot-foot toe prosthesis.

干预措施: silicone foot and foot toe prosthesis (Device)

结局指标

主要结局

Nottingham Health Profile (NHP)

时间窗: through study completion, an average of 1 year

The NHP questionnaire consists of two sections with "Yes-No" responses. The first section includes dimensions such as energy levels, pain, emotional reactions, sleep, social isolation, and physical abilities, while the second section addresses the impact of poor health on daily life, covering areas such as employment, household activities, social life, relationships, sexual life, hobbies, and vacations. The first section's total score ranges from 0-600, with higher scores indicating lower activity. The second section ranges from 0-7, with higher scores indicating lower activity.

Trinity Amputation and Prosthesis Experience Scales (TAPES)

时间窗: through study completion, an average of 1 year

The TAPES questionnaire evaluates psychosocial adaptation, functionality, and prosthesis satisfaction. It comprises two main sections with nine subscales. The psychosocial subscales include general adaptation, social adaptation, and restriction adaptation, with each rated on a five-point scale (1: Strongly Disagree to 5: Strongly Agree). Scores range from 5 to 25, with higher scores indicating better adaptation.

Visual Analog Scale(VAS)

时间窗: through study completion, an average of 1 year

The VAS was used to measure pain in the stump before and after silicone prosthesis use. They were asked to draw their pain level on a 10 cm scale between 0-10 points as 0=no pain, 10 unbearable pain

次要结局

未报告次要终点

研究者

发起方
Medipol University
申办方类型
Other
责任方
Principal Investigator
主要研究者

ESRA ATILGAN

Assoc.Prof.Dr.

Medipol University

研究点 (1)

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