Typing Proficiency Following Carpal Tunnel Release
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Carpal tunnel syndrome is a condition in which the median nerve is compressed at the wrist. It causes such symptoms as numbness, tingling, weakness, muscle damage, and pain. If non-operative treatments do not work generally patients go on to carpal tunnel release surgery in which the transverse carpal ligament is released. After surgery patients usually return to work with no restrictions within six weeks. Patients often ask how soon they are able to return to typing after surgery, and what their typing ability will be like after surgery. Currently there are no studies that evaluate how long it takes for patient's typing skills to return to that of the pre-operative skill level. We would like to answer that question by comparing typing results from different time points including a baseline prior to surgery. We additionally seek to identify which patient characteristics are predictive of a faster return of typing proficiency.
An additional innovative aspect of this project is the use of a web-based typing test that will be used in the assessment of patient typing proficiency. We will additionally use a web-based model for the collection of our survey data.
Type d'étude
Inscription (Réel)
Contacts et emplacements
Lieux d'étude
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Tennessee
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Nashville, Tennessee, États-Unis, 37232
- Vanderbilt University Hand & Upper Extremity Center
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
Méthode d'échantillonnage
Population étudiée
La description
Inclusion Criteria:
- Patients set to undergo carpal tunnel release
- Patients who have a positive EMG test
- Patients must have access to a computer with internet access
- Patients must have an email account
- Patients must be between the ages of 20-70
Patients that meet typing test requirements
- Must type weekly
- Typing proficiency of 30 wpm at time of pre-operative appointment
- Must use all fingers when typing
- Can read text in font Times New Roman size 14
Exclusion Criteria:
- People who cannot read or write
- People who do not meet inclusion criteria
- Patients who do not speak English
- Patients unwilling or unable to return for follow-up visits prescribed by the study protocol
- Patients who qualify for inclusion in the study, but refuse to participate.
- Patients with concurrent, ipsilateral confounding hand or upper extremity pathology such as trigger finger, ganglion cyst, painful arthritis, etc.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Cohortes et interventions
Groupe / Cohorte |
Intervention / Traitement |
|---|---|
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Patients who have carpal tunnel release surgery
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Change in typing test measurements (speed and accuracy)
Délai: Preoperative, Postoperative: 8-10days, 2wks, 3wks, 4wks, 5wks, 6wks, 8wks, 12wks
|
Each patient will complete a preoperative typing test (at their home) prior to undergoing carpal tunnel release surgery.
The patient will then take the same typing test at the following time points postoperatively: 8-10days, 2wks, 3wks, 4wks, 5wks, 6wks, 8wks, 12wks.
The change in speed and accuracy will be assessed by comparing the preoperative (baseline) typing test results to the postoperative typing test results.
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Preoperative, Postoperative: 8-10days, 2wks, 3wks, 4wks, 5wks, 6wks, 8wks, 12wks
|
Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Les enquêteurs
- Chercheur principal: Donald H Lee, MD, Vanderbilt University
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Estimation)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 101131
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