NCT06754241

Brief Summary

To investigate the impact of personalized rehabilitation guidance based on the WeChat Official Accounts Platform on the functional recovery and quality of life of patients with knee osteoarthritis (KOA).Ninety patients diagnosed with KOA undergoing joint replacement were included via convenient sampling.The patients were randomly divided into an observation group and a control group,with 45 patients in each group.The control group received traditional rehabilitation guidance,while the observation group received personalized rehabilitation guidance through the WeChat Official Accounts Platform in addition to the traditional guidance.Different care plans had varying effects on patients' scores on the 36-item Short Form Health Survey (SF-36),Visual Analog Scale (VAS),and Lysholm Knee Scoring Scale.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
90

participants targeted

Target at P50-P75 for not_applicable knee-osteoarthritis

Timeline
Completed

Started Jan 2024

Shorter than P25 for not_applicable knee-osteoarthritis

Geographic Reach
1 country

1 active site

Status
completed

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 Start

First participant enrolled

January 1, 2024

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 15, 2024

Completed
17 days until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2024

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

December 18, 2024

Completed
13 days until next milestone

First Posted

Study publicly available on registry

December 31, 2024

Completed
Last Updated

December 31, 2024

Status Verified

September 1, 2024

Enrollment Period

8 months

First QC Date

December 18, 2024

Last Update Submit

December 23, 2024

Conditions

Outcome Measures

Primary Outcomes (4)

  • The 36-item Short Form Health Survey (SF-36)

    The SF-36 is a concise health survey divided into 8 subscales: physical function, role physical, bodily pain, global health, vitality, social function, role emotional, and mental health, where a higher score indicates a better health status.

    at 1 week and 1 month post-discharge

  • Visual Analog Scale (VAS)

    The VAS was used to assess pain levels before and after treatment in the two groups. VAS scores are positively correlated with pain intensity, where 0 indicates no pain and 10 indicates the most severe pain. A score of ≤3 is defined as mild pain, 4-6 as moderate pain, and ≥7 as severe pain.

    at 1 week and 1 month post-discharge

  • Lysholm Knee Scoring Scale

    The Lysholm Knee Scoring Scale was employed to evaluate knee function. This scale covers eight aspects, including limping, support, restraining, instability, pain, swelling, climbing stairs, and squatting. It is scored on a scale of 0 to 100. The total score is 100 points, with higher scores indicating fewer symptoms and higher levels of functioning. A score above 95 is considered excellent, 85-94 is good, 65-84 is fair, and less than 65 is poor.

    at 1 week and 1 month post-discharge

  • The Newcastle Satisfaction with Nursing Scale (NSNS)

    The Newcastle Satisfaction with Nursing Scale (NSNS) was used to measure patient satisfaction with nursing care. This scale consists of 19 items, such as nurse competence, communication, emotional support, and safety management. Each item is rated on a scale of 1-5, with a total score ranging from 19 to 95 points. A score of ≥77 indicates very satisfied, 58-76 indicates satisfied, 39-57 indicates moderately satisfied, and ≤38 indicates dissatisfied.

    at 1 week and 1 month post-discharge

Study Arms (2)

control group

ACTIVE COMPARATOR
Behavioral: conventional nursing care

observation group

EXPERIMENTAL
Behavioral: Intervention Care

Interventions

(1) Preoperative education: An appropriate walking aid was provided for the patient and instructions were given to guide correct use, while isometric muscle exercises were taught. (2) Postoperative care: Six hours after anesthesia recovery, the head of the patient's bed could be elevated as needed, and the patient was instructed to perform ankle pumps (dorsiflexion and plantarflexion of the ankle).(3) Postoperative exercise: One to two days after surgery, following the removal of the drainage tube, the patient was encouraged to continue with ankle pumps and isometric quadriceps contractions, as well as to begin straight-leg raises. (4) Postoperative Day 3: In strict accordance with medical advice and under the guidance of a physiotherapist, patients engaged in continuous passive motion therapy for the affected knee, along with manual knee joint massage. (5) Postoperative Days 5-7: the patient would try to stand with the assistance of a walker, gradually progressing to walking exercises

control group

(1) Intervention Day 1: (i) All patients in the observation group were provided with an introduction to the study and invited to join the WeChat group for the observation group. (2) Intervention Day 2: Exercise guidance for patients with KOA was shared via the WeChat group.(3) Intervention Day 3: Guidance for emotional regulation was sent to the patients with KOA via the WeChat group.(4) Intervention Week 1: A micro-lesson on KOA-related knowledge was delivered via the WeChat group to deepen patients' understanding. (5) Intervention Week 2: (i) Text instructions and related questions on common conservative treatments for KOA, including topical and oral painkillers, were shared, with correct answers provided the next day.(ii) A micro-lesson on exercise guidance for patients with KOA was uploaded to the WeChat group to reinforce patients' understanding.

observation group

Eligibility Criteria

Age50 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • aged 50 to 80 years;
  • conscious, without cognitive impairments, and able to complete reading independently or with assistance;
  • able to operate a smartphone and use WeChat;
  • willing to participate in this study and provide signed informed consent.

You may not qualify if:

  • acute cerebrovascular disease with sequelae in the past 6 months;
  • coexisting primary psychiatric disorders;
  • unable to perform physical exercise due to physical disability in the lower limbs;
  • postoperative complications, such as deep vein thrombosis or infection;
  • participation in other interventional studies.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Fuyang Hospital of Anhui Medical University

Fuyang, Anhui, 236000, China

Location

Related Publications (1)

  • Li X, Jiang S, Zhou M, Dong Y. WeChat-Based Personalized Rehabilitation: Enhancing Recovery and Quality of Life in Knee Osteoarthritis. Nurs Health Sci. 2025 Jun;27(2):e70149. doi: 10.1111/nhs.70149.

MeSH Terms

Conditions

Osteoarthritis, Knee

Condition Hierarchy (Ancestors)

OsteoarthritisArthritisJoint DiseasesMusculoskeletal DiseasesRheumatic Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

December 18, 2024

First Posted

December 31, 2024

Study Start

January 1, 2024

Primary Completion

August 15, 2024

Study Completion

September 1, 2024

Last Updated

December 31, 2024

Record last verified: 2024-09

Data Sharing

IPD Sharing
Will not share

Locations