NCT07422714

Brief Summary

A Comparative Study of Traditional Rehabilitation and Remote Intelligent Rehabilitation: Exploring the Application Effectiveness of Intelligent Rehabilitation in Frozen Shoulder Rehabilitation

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
42

participants targeted

Target at P25-P50 for not_applicable

Timeline
3mo left

Started Jan 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress55%
Jan 2026Aug 2026

First Submitted

Initial submission to the registry

January 21, 2026

Completed
Same day until next milestone

Study Start

First participant enrolled

January 21, 2026

Completed
1 month until next milestone

First Posted

Study publicly available on registry

February 20, 2026

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 31, 2026

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 30, 2026

Expected
Last Updated

February 20, 2026

Status Verified

January 1, 2026

Enrollment Period

2 months

First QC Date

January 21, 2026

Last Update Submit

February 13, 2026

Conditions

Range of Motion, Articular

Keywords

Frozen ShoulderSmart rehabilitationfunctional exercise

Outcome Measures

Primary Outcomes (1)

  • Constant-Murley Shoulder Assessment Score Scale

    The Constant-Murley Shoulder Assessment Score Scale consists of four components: activities of daily living (20 points), pain (15 points), muscle strength (25 points), and range of motion (40 points), with a total score of 100 points. A lower score indicates a higher percentage of dysfunction, while a higher score indicates the opposite. The questionnaire demonstrates high accuracy and reliability and is commonly used to assess patients' shoulder joint conditions.

    Week 0、Week 4 and Week 8

Secondary Outcomes (5)

  • Visual Analogue Scale

    Week 0、Week 4 and Week 8

  • Shoulder Range of Motion

    Week 0、Week 4 and Week 8

  • Shoulder muscle strength

    Week 0 、Week 4 and Week 8

  • Shoulder joint MRI

    Week 0 、Week 4 and Week 8

  • Exercise completion rate

    Week 0 、Week 4 and Week 8

Study Arms (3)

Experimental group

EXPERIMENTAL

Combination of traditional rehabilitation and intelligent rehabilitation

Other: Artificial and intelligent combination of shoulder joint function exercise

Traditional rehabilitation group

EXPERIMENTAL

Rehabilitation training by a rehabilitation therapist

Other: Traditional rehabilitation training

Smart rehabilitation group

EXPERIMENTAL
Other: Intelligent rehabilitation training

Interventions

Artificial and intelligent combination of shoulder joint function exerciseOTHER

Rehabilitation therapist rehabilitation and intelligent rehabilitation are combined

Also known as: Experimental group
Experimental group
Traditional rehabilitation trainingOTHER

Shoulder joint function training is performed by a rehabilitation therapist

Traditional rehabilitation group
Intelligent rehabilitation trainingOTHER

Shoulder joint rehabilitation training is carried out according to the intelligent rehabilitation system

Smart rehabilitation group

Eligibility Criteria

Age40 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Diagnosed with the adhesive phase of frozen shoulder by the Department of Sports Medicine, with patients potentially coming from different physicians;
  • Have not participated in any other clinical trials within the past 3 months; ④ Patients voluntarily agree to participate in the clinical trial, sign the informed consent form, and are able to cooperate with clinical follow-up.

You may not qualify if:

  • Patients with local lesions in the affected shoulder or arm, such as skin damage, infection, tuberculosis, tumors, or skin diseases;
  • Patients with poor physical condition who are unable to tolerate the intensity of rehabilitation training; ④ Patients with cognitive impairments who cannot undergo normal rehabilitation training, or other conditions deemed by the physician as unsuitable for trial participation; ⑤ Pregnant or breastfeeding women; ⑥ Patients with other shoulder conditions, such as rotator cuff tears or shoulder dislocation.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Peking University Third Hospital

Beijing, China

RECRUITING

MeSH Terms

Conditions

Bursitis

Condition Hierarchy (Ancestors)

Joint DiseasesMusculoskeletal Diseases

Central Study Contacts

Zhenlong Liu

CONTACT

13261993917zhenlong_liu@bjmu.edu.cn

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 21, 2026

First Posted

February 20, 2026

Study Start

January 21, 2026

Primary Completion

March 31, 2026

Study Completion (Estimated)

August 30, 2026

Last Updated

February 20, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

Locations

CN(1)