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Clinical Trials in France / NCT07671430
Recruiting Not applicable

Assessment of the Benefits of Psychological Care Before Anterior Cruciate Ligament Surgery of the Knee (CLIPPER)

NCT07671430 · tracked via the Priya Life Science France tracker
Sponsor
GCS Ramsay Santé pour l'Enseignement et la Recherche
Phase
Not applicable
Started
2026-05-07
Last updated
2026-06-26

Condition(s) studied

AnxietyLigament Reconstruction Surgery

Investigational drug(s) / intervention(s)

A consultation with a psychologist prior to surgery

A consultation with a psychologist prior to surgery: A videoconference consultation with a psychologist prior to surgery

Study summary

The primary objective of this study is to assess the impact of a preoperative psychological consultation on postoperative pain in anxious patients undergoing primary anterior cruciate ligament reconstruction surgery.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patient having signed the consent form for participation in the study * Patient scheduled for first-line outpatient ACL reconstruction surgery * Patient with a score \>30 on the SFQ questionnaire (which assesses fear of surgery) * Patient with the ability to connect to the internet and follow a teleconsultation on a screen Exclusion Criteria: * Surgical history of the operated knee * History of psychiatric disorders and/or regular use of psychotropic medication * Regular use of opioid medication * Mental disability or any other reason that may hinder understanding or strict adherence to the protocol * Patient not affiliated with the French social security system * Patient under legal protection, guardianship or curatorship * Pregnant, breastfeeding or childbearing women without effective contraception * A patient who is already enrolled in another therapeutic study protocol or who has participated in another trial within the past three months

Primary outcome measure(s)

  • Compare the intensity of postoperative pain between the two groups during the night following the procedure — First night following surgery
    The maximum pain intensity experienced during the first night after surgery is measured using a numerical rating scale (NRS)

Trial sites (1)

FacilityCityRegionStatus
clinique du Sport Paris France Recruiting

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Other trials for the same condition

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Randomized, Single-blind Pilot Study Assessing the Effect of Cutaneous RESonance Stimulation SYMPAthetic and Parasympathetic Tone and Anxiety in Patients Admitted for Cardiac Surgery Recruiting
A Study of the Impact of a Virtual Reality Medical Device (HypnoVR® Headset) on Anxiety and Pain in Interventional Radiology. Starting soon
Immersive Virtual Reality for the Management of Anxiety Among Nurses Recruiting
Evaluation of the Effectiveness of Music Therapy on Anxiety Levels in Patients With Advanced Cancer Hospitalized in a Palliative Care Unit Starting soon
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07671430 on ClinicalTrials.gov ↗ ← All trials in France