Telerehabilitation for Anterior Cruciate Ligament Reconstruction - TAR Program in Adolescents

Anterior Cruciate Ligament Injuries Clinical Trial

— TAR  

Official title:

Feasibility and Effectiveness of Telerehabilitation for Anterior Cruciate Ligament Reconstruction - TAR Program Involving a Motion Capture Mobile Application in Adolescents: A Pilot Randomised Controlled Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05799235
• Other study ID #: 2022/2379
• Status: Recruiting
• Phase: N/A
• Start date: February 15, 2023
• Est. completion date: April 30, 2025

Study information

• Verified date: March 2023
• Source: KK Women's and Children's Hospital
• Contact: Cheri Chan
• Phone: +65 6225 5554
• Email: cheri.chan.s.h[@]kkh.com.sg
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 40
• Est. completion date: April 30, 2025
• Est. primary completion date: October 31, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 12 Years to 20 Years

Eligibility

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

Related Conditions & MeSH terms

• Anterior Cruciate Ligament
• Anterior Cruciate Ligament Injuries
• Telerehabilitation

Intervention

Device:
• Telerehabilitation TAR program using a mobile application
Participants in this study arm will use a mobile application which allows participants to perform their home exercises with real-time feedback given, allowing for proper execution of exercises, on top of standard care.

Other:
• Standard rehabilitation sessions
Participants in this control group will attend standard in person rehabilitation sessions with home exercise program given as per standard care.

Locations

Country	Name	City	State
Singapore	KK Women's and Children's Hospital	Singapore

Sponsors (1)

Lead Sponsor	Collaborator
KK Women's and Children's Hospital

Country where clinical trial is conducted

Singapore, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Exercise adherence	This will be measured via the Exercise Adherence Rating Scale (via the 6 item questions on assessing adherence to prescribed home exercises) over 12 weeks post-operatively, via changes in scores over the time points. The scores will range from 0-24, with higher scores indicating higher adherence.	Post-operatively: Week 3, Week 6, Week 9, Week 12
Secondary	Pain intensity	Pain at rest and with movement will be measured on a 11-point numeric pain rating scale, with zero representing no pain at all and 10 representing worst imaginable pain.	Pre-operatively (=one month prior to operation), Post-operatively: Week 3, Week 6, Week 9, Week 12
Secondary	Range of motion	A goniometer will be used to measure knee range of motion.	Pre-operatively (=one month prior to operation), Post-operatively: Week 3, Week 6, Week 9, Week 12
Secondary	Quadriceps and hamstring strength	Strength for quadriceps and hamstring will be obtained using the knee flexion extension machine (isotonic isometric).	Pre-operatively (=one month prior to operation), Post-operatively: Week 6, Week 12
Secondary	One leg sit to stand	One leg sit to stand test will be conducted with a standard chair height, with one leg sit to stand rate calculated.	Pre-operatively (=one month prior to operation), Post-operatively: Week 6, Week 12
Secondary	Self-reported function	Pedi-IKDC (Pediatric version of the International Knee Documentation Committee) questionnaire will be used to measure their self-reported lower limb function (scores range from 0-100, with higher scores indicating lower function or greater symptoms).	Pre-operatively (=one month prior to operation), Post-operatively: Week 6, Week 12
Secondary	Self-reported quality of life	EQ-5D-Y (child-friendly EQ-5D version) quality of life questionnaire consists of two sections. First section covers five health domains: mobility, self-care, usual activities, pain or discomfort and feeling worried, sad or unhappy, with each domain responses as no problems, some problems and a lot of problems. The response categories will be reflected by a 1-digit number (1-3) and combined into a 5-digit number based on the domains to describe their health state.; The second section cover the EQ VAS, which requires rating of their health between 100 (the best health you can imagine) and 0 (the worst health you can imagine).	Pre-operatively (=one month prior to operation), Post-operatively: Week 6, Week 12
Secondary	Motivation	Treatment self-regulation questionnaire will be used to measure their self-determination/ motivation to exercise regularly. It consists of 15 questions on a 7-point scale from 'not at all true' to 'very true'. Scores for each question range from 1 to 7, with higher scores indicating the more dominant motivational style.	Pre-operatively (=one month prior to operation), Post-operatively: Week 6, Week 12
Secondary	Perceived competence	Perceived competence scale will be used to measure their perceived confidence to exercise regularly. It consists of four questions on a 7-point scale from 'not at all true' to 'very true'. Total scores range from 4 to 28, with higher scores indicating greater perceived confidence.	Pre-operatively (=one month prior to operation), Post-operatively: Week 6, Week 12
Secondary	Treatment satisfaction	A 11-point numeric rating scale will be used for participants to rate their satisfaction and convenience of treatment received, with zero indicating not satisfied at all/ not convenient at all and 10 indicating completely satisfied/ most convenient.	Post-operatively: Week 6, Week 12
Secondary	Number of face to face rehabilitation session	Number of in person rehabilitation sessions	Post-operatively: Week 12
Secondary	mHealth App Usability Questionnaire (MAUQ)	This will be used with participants in the intervention group to gather feedback and determine usability of the use of this mobile application for home-based rehabilitation post ACLR. Each survey question consists of a Likert scale rating (on a scale of five), with higher scores indicating greater ease of use and satisfaction, system information arrangement, usefulness and intention to use.	Post-operatively: Week 12