Effects of Acupuncture-assisted Rehabilitation Protocol for Achilles Tendon Rupture

Sponsor
Peking University Third Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05957614
Collaborator
(none)
200
2
23.6

Study Details

Study Description

Brief Summary

This prospective study is to compare the rehabilitation effect between the patients with achilles tendon rupture using traditional rehabilitation protocol and acupuncture-assisted rehabilitation protocol. The main question it aims to answer is whether acupuncture is an effective rehabilitation treatment. The patients are divided into the traditional rehabilitation group and acupuncture assisted rehabilitation group. The time of return to light sports activity and other indicators of the two groups will be compared.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Traditional rehabilitation protocol
  • Procedure: Acupuncture-assisted Rehabilitation Protocol
N/A

Detailed Description

This prospective randomized controlled clinical study is designed to compare the treatment outcomes of different rehabilitation protocols by dividing the patients into two groups-based on the traditional rehabilitation protocol and acupuncture-assisted rehabilitation protocol. See the text for detailed inclusion and exclusion criteria. Patients that meet all the inclusion criteria but do not meet any exclusion criteria, and who have signed the informed consent will be recruited, and each patient will be assigned a unique patient identification number, which will be used throughout the study identify the patient. All patients be treated surgically with the same suture technique. For acupuncture-assisted rehabilitation group, patients will receive additional acupuncture treatment. Investigators will collect indicators from multiple dimensions such as ankle function and pain level to compare the efficacy of the two groups.

The achilles tendon , despite being the largest and strongest tendon, is often prone to ruptures. The latest evidence48 has demonstrated that at centers using functional rehabilitation, nonoperative treatment results in similar rerupture rates but significantly lower complica- tion rates than surgical treatment. So we expect this trial to point out better rehabilitation.

In traditional Chinese acupuncture, nearly 400 acupoints on the body surface are interrelated to various functions. Acupuncture has also been widely studied for the treatment of motor system diseases. However, trials on rehabilitation of Achilles tendon rupture are still lacking.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Prospective Randomized Controlled Clinical Trial on the Comparison of Traditional Rehabilitation Protocol and Acupuncture-assisted Rehabilitation Protocol for Achilles Tendon Rupture
Anticipated Study Start Date :
Jul 15, 2023
Anticipated Primary Completion Date :
Jun 1, 2025
Anticipated Study Completion Date :
Jul 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Traditional Rehabilitation Protocol

Procedure: Traditional rehabilitation protocol
Rehabilitation protocol after open surgery for Achilles tendon rupture, including immobilization, early weightbearing ankle motion exercise and isolated early ankle motion exercises.

Active Comparator: Acupuncture-assisted Rehabilitation Protocol

Procedure: Acupuncture-assisted Rehabilitation Protocol
Add acupuncture treatment on the basis of traditional rehabilitation protocol.The acupuncture procedure is as follows, acupuncture treatment is carried out for half an hour every day in two weeks after surgery. The acupoints on the affected side are ST36(ZuSanLi), GB34(YangLingQuan) and SP9(YinLingQuan), and the acupoints on the healthy side are Ki3(TaiXi), bl60(KunLun) and PC7(DaLing).

Outcome Measures

Primary Outcome Measures

  1. The time of return to light sports activity [From operation to 1-year follow-up after the surgery]

    When the patients are able to do jogging or rapid walk after the surgery, the time will be recorded.

Secondary Outcome Measures

  1. Range of motion (ROM) recovery time [From operation to 1-year follow-up after the surgery]

    The recovery time will be recorded when the ROM is similar to that of the uninjured side.

  2. Recovery time of the single-legged heel rise height (SHRH) [From operation to 1-year follow-up after the surgery]

    The heel rise height is measured as the distance from the ground to the heel when the patient lift the heel while keeping the knee straight. The recovery time is noted when the SHRH is similar to that of the opposite leg.

Other Outcome Measures

  1. Visual analogue scale (VAS) [2, 4, 6, 8, 10, 12, 14, 16, 24, and 48 weeks after the surgery]

    VAS pain score is from 0 to 10, the higher score demonstrate the more severe.

  2. American Orthopaedic Foot and Ankle Society (AOFAS) hindfoot score [2, 4, 6, 8, 10, 12, 14, 16, 24, and 48 weeks after the surgery]

    The AOFAS score ranges from 0 to 100, with a healthy hindfoot receiving 100 points.

  3. The Achilles tendon Total Rupture Score (ATRS) [2, 4, 6, 8, 10, 12, 14, 16, 24, and 48 weeks after the surgery]

    The ATRS includes 10 items; each item has a score ranging between 0 and 10 on a Likert scale, with 100 indicating no major limitations.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • acute closed single-legged complete Achilles tendon rupture

  • age of 18 to 60 years.

Exclusion Criteria:
  • patients with prior Achilles tendon rupture or other situations that affected their lower limb functions or tendon healing (e.g., autoimmune disease, diabetes mellitus, systemic corticosteroid treatment).

  • an inability to complete our suture technique (e.g., the distance from the rupture site to the Achilles tendon insertion was less than 3.5 cm) .

  • those without rehabilitation or follow-up outcomes.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Peking University Third Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Peking University Third Hospital
ClinicalTrials.gov Identifier:
NCT05957614
Other Study ID Numbers:
  • PekingUTHLYBLY
First Posted:
Jul 24, 2023
Last Update Posted:
Jul 24, 2023
Last Verified:
Jun 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Peking University Third Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 24, 2023