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Video-Based Education Versus In-Person Education in Patients Undergoing Arthroscopic Partial Meniscectomy

Effectiveness of a Video-Based Educational Intervention Compared With In-Person Education on Psychosocial and Functional Outcomes in Patients Undergoing Arthroscopic Partial Meniscectomy: A Noninferiority Randomized Controlled Trial

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07358325
Acronym
NI-RCT
Enrollment
166
Registered
2026-01-22
Start date
2026-01-19
Completion date
2026-06-01
Last updated
2026-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Knee Arthroscopic Surgery, Partial Meniscectomy

Brief summary

The primary aim of the study is to investigate whether video-based education and exercise-program is non-inferior to in-person instructions in improving pain-related self-efficacy in patients undergoing arthroscopic partial meniscectomy in a day-hospital setting. Secondary aims are to explore the potential superiority of the video-based program compared to in-person instructions in reducing disability and kinesiophobia in the same patient population.

Interventions

The video-based education was sent to patients within 5-day before surgery and consists of instructions to follow after surgery on wight-baring on the operated limb, advice to reduce swelling and movements tallowed to be performed. Exercises to perform in the 2 weeks after surgery are shown.

BEHAVIORALUsual Care

Immediately after the surgery in day-hospital setting, a physiotherapist provided in-person instructions to patients assigned to control group. Instructions consists of the same educational content of the video-based group and the same exercises to perform in 2-weeks after surgery are shown and provided on a written spreadsheet.

Sponsors

Istituto Clinico Humanitas
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients scheduled for arthroscopic partial meniscectomy (medial or lateral meniscus) performed in a day-hospital setting. * Traumatic or degenerative meniscal tears. * Treatment at the Hip and Knee Orthopedic Unit of the Humanitas Clinical Institute. * Age ≥ 18 years. * Access to adequate video support. * Sufficient proficiency in the Italian language.

Exclusion criteria

* Previous surgery on either knee within the past 5 years. * Significant postoperative hematoma requiring aspiration. * Neurological conditions potentially affecting functional or motor recovery. * Musculoskeletal conditions potentially affecting functional or motor recovery. * Rheumatologic conditions potentially affecting functional or motor recovery. * Internal medicine conditions potentially affecting functional or motor recovery. * Oncological conditions potentially affecting functional or motor recovery. * Cognitive or psychiatric disorders (Mini-Mental State Examination ≤ 21).

Design outcomes

Primary

MeasureTime frameDescription
Pain Self-Efficacy Questionnaire (PSEQ)From enrolment to the 6 weeks after surgeryThe PSEQ assesses patients' confidence in performing daily activities despite pain, with score ranging from 0 to 60 and higher scores indicating greater pain-related self-efficacy.

Secondary

MeasureTime frameDescription
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)From enrolment to the 3 weeks after surgeryThe WOMAC evaluates knee pain, stiffness, and physical function, with score ranging from 0 to 96 and higher scores reflecting greater pain and functional impairment.
Tampa Scale of Kinesiophobia (TSK)From enrolment to the 3 weeks after surgeryThe TSK measures fear of movement and re-injury related to pain, with score ranging from 17 to 68 and higher scores indicating greater levels of kinesiophobia.
Pain Self-Efficacy Questionnaire (PSEQ)From enrolment to the 3 weeks after surgeryThe PSEQ assesses patients' confidence in performing daily activities despite pain, with score ranging from 0 to 60 and higher scores indicating greater pain-related self-efficacy.

Countries

Italy

Contacts

CONTACTRoberto Gatti
roberto.gatti@hunimed.eu+390282245610

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026