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Telerehabilitation for Anterior Cruciate Ligament Reconstruction - TAR Program in Adolescents

K

KK Women's and Children's Hospital

Status

Enrolling

Conditions

Anterior Cruciate Ligament Injuries
Telerehabilitation
Anterior Cruciate Ligament

Treatments

Other: Standard rehabilitation sessions
Device: Telerehabilitation TAR program using a mobile application

Study type

Interventional

Funder types

Other

Identifiers

NCT05799235
2022/2379

Details and patient eligibility

About

Anterior cruciate ligament (ACL) injuries are common in adolescents and its prevalence has increased over the years, especially with more adolescents engaging in physical activities and competitive sports. Standard of care for these injuries would be an ACL reconstruction (ACLR) to allow return to function and sports and reduce the risk of post-traumatic arthritis and recurrent knee injuries. Rehabilitation post-ACLR is crucial to optimise surgical outcomes and prevent re-rupture of ACL. However, good compliance to rehabilitation is often a challenge for patients and healthcare providers.

Telerehabilitation for this group of patients may help to augment rehabilitation by improving patient compliance and overcome barriers to behavioural change often observed in traditional in-person physiotherapy. It can also allow remote monitoring and provide feedback to patients during exercises. In addition, it is a useful tool during pandemic when in-person visits are not possible. Currently, very few studies have evaluated the use of telerehabilitation with remote monitoring for ACLR, especially in adolescents. The use of home-based telerehabilitation post ACLR may be key to improving patient motivation and exercise compliance in adolescents.

For this pilot study, the intervention group will undergo the TAR program in addition to standard care, which involves self-administered exercises in initial 12 weeks post ACLR using a mobile application. The mobile application will detect key landmarks on the body for human pose estimation. Participants will be able to perform their exercises with real-time feedback given, allowing for proper execution of the exercises. Exercise adherence, range of motion and pain scores will be tracked via the application and therapists are able to monitor via the online dashboard. The control group will undergo standard in-person physiotherapy.

Primary aim of this study is to examine exercise adherence in TAR program versus standard care post ACLR in adolescents. Secondary aims of this study are to examine the effects of TAR program on knee strength, range, function, quality of life, treatment satisfaction, self-determination and number of face-to-face rehabilitation sessions required after ACLR.

Enrollment

40 estimated patients

Sex

All

Ages

12 to 20 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participants age 12 to 20 years old
  • Participants undergoing ACLR surgery
  • Participants willing to be included in either the intervention group (utilizing the mobile application) or control group

Exclusion criteria

  • Participants with complications after ACLR surgery
  • Participants with significant neurological or other lower limb impairments or conditions affecting mobility and function
  • Participants with previous ACL surgeries of the same affected lower limb
  • Participants with previous surgeries or trauma to the unaffected lower limb

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 2 patient groups

Telerehabilitation TAR program using a mobile application (intervention group)
Experimental group
Description:
Participants in the intervention group will undergo the telerehabilitation TAR program and install and utilise the application on their mobile device, and self-administer the home exercises as prescribed by their physiotherapists. The mobile application uses novel deep learning algorithm on a mobile platform to detect key landmarks on the body for human pose estimation. Participants will be able to perform their rehabilitation exercise with real-time feedback allowing for proper execution of the exercises. The participants will be instructed on the installation and use of the mobile application and will be expected to perform the prescribed exercises independently (using the application) as instructed by their Physiotherapists. This application will be used for the initial 12 weeks of post-op rehabilitation.
Treatment:
Device: Telerehabilitation TAR program using a mobile application
Standard rehabilitation (control group)
Active Comparator group
Description:
Participants in the control group will attend standard in person rehabilitation sessions at the outpatient clinic. Participants will be prescribed a home exercise program as per standard care.
Treatment:
Other: Standard rehabilitation sessions

Trial contacts and locations

1

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Central trial contact

Cheri Chan

Data sourced from clinicaltrials.gov

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