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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03872193
Other study ID # Virtual Reality Physiotherapy
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 10, 2016
Est. completion date June 10, 2018

Study information

Verified date March 2019
Source Hacettepe University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to compare the effects of virtual reality applications on quality of life, performance, balance, prosthesis adaptation and gait parameters in individuals with transtibial amputation. 20 Transtibial amputee were included in study. All participants were using transtibial prothesis with active vacuum system at least 1 year. Participants were divided into two groups. While a group of virtual reality applications were being performed additionally standart physiotherapy, only standard physiotherapy methods were applied in the second group. Balance and gait practices were performed for each group. Individuals were treated for 3 days a week for 4 weeks, and individuals were evaluated before and after treatment. Individuals were evaluated for quality of life, performance, balance, prosthesis adaptation and time-distance parameters of walking.


Description:

The aim of this study is to compare the effects of virtual reality applications on quality of life, performance, balance, prosthesis adaptation and gait parameters in individuals with transtibial amputation.20 transtibial amputee with 36 mean age were included in study. All participants were using transtibial prothesis with active vacuum system at least 1 year. Participants were divided into two groups. While a group of virtual reality applications were being performed, standard physiotherapy methods were applied in the second group. Balance and gait practices were performed for each group. Individuals were treated for 3 days a week for 4 weeks, and individuals were evaluated before and after treatment. Individuals were evaluated for quality of life, performance, balance, prosthesis adaptation and time-distance parameters of walking.

For this purpose, SF-36 Questionnaire, 6-minute walking test, one leg rest time, Trinity Amputation and Prosthetic Experience Scale, wearable biometric device and footprint method were utilized. There was a statistically significant difference between the two groups in pre-treatment and post-treatment performance, balance and gait parameters in the groups of individuals (p <0.05). The quality of life pain parameter was statistically decline in the group receiving virtual reality (p<0.05). On the other hand, significant differences in the quality of life and prosthesis adaptation of the individuals were not found between the groups (p> 0.05). The results of this study showed that virtual reality practices and standard physiotherapy methods are effective on performance, balance and walking in transtibial amputee rehabilitation. It is thought that it will be important to perform virtual reality applications in amputee rehabilitation separately in both methods, in addition to standard physiotherapy methods, to include in rehabilitation process, to bring an ability of alternative application to professionals working in this area and to work about amputees with using different suspension systems and with different amputation levels.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date June 10, 2018
Est. primary completion date March 12, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- transtibial and unilateral amputation

- At least 1 year prothesis usage, 18- 65 year age,

- At least 15 min independent walking ability,

- Stabile stump volume,

- Standart stump lentgh,

- Enough kognition for evaluation and tests.

Exclusion Criteria:

- walking and other activities to prevent; shortness of muscle, limitation of joint motion and phantom pain in stump, presence of any discomfort or systemic health problem that may affect the gait outside the amputation

- presence of visual problems to prevent participation in virtual reality applications,

- use of walking aids

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Exercise
Virtual Reality Exercies

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Hacettepe University

Outcome

Type Measure Description Time frame Safety issue
Primary Quality of Life measured of individuals: SF-36 Scale SF-36 Quality of Life Scale, higher values represent a better 10 minute
Primary Balance Test Single Leg Balance Test,higher values represent a better 5 minute
Primary Performance Test 6 minute walk test,higher values represent a better 6 minute
Primary Prothesis Satisfaction: Trinity Amputation Prothesis Experience Scale Trinity Amputation Prothesis Experience Scale; 5 point likert scale,5-75 point, activity limitation,physicosocial adaptation,prothesis satisfaction 5 minute
Primary Gait Parameters Wearable Biometric Device 6 minute
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