- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT02438384
Patient Education to Improve Pain Management in Older Adults With Acute Musculoskeletal Pain: A Pilot Randomized Trial (BETTER_Pilot)
This is a three arm pilot randomized trial. Patients will be assigned to:
- Usual care
- Video education in the Emergency Department (ED)
- Video education in the ED plus phone follow-up at three days with geriatric pain management specialist for all patients with pain >=4/10
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
This is a three arm pilot randomized trial. Patients will be assigned to:
- Usual care
- Video education in the ED (10 minute interactive video)
- Video education in the ED plus phone follow-up at three days with geriatric pain management specialist for all patients with pain >=4/10
Type d'étude
Inscription (Réel)
Phase
- N'est pas applicable
Contacts et emplacements
Lieux d'étude
-
-
North Carolina
-
Chapel Hill, North Carolina, États-Unis, 27599
- UNC Hospitals Emergency Department
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- Age 50 and older; ED visit for acute musculoskeletal pain
Exclusion Criteria:
- Cognitively impaired; chronic pain (daily opioid use prior to onset of pain or pain symptoms more than one month); prison; injury or pain condition requiring hospital admission.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
---|---|
Aucune intervention: Usual care
Pts will receive education and follow-up based on judgment of emergency provider.
|
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Expérimental: Video
Patients will watch 10 minute educational video
|
This is a 10 minute interactive video which provided information to the viewer regarding the safe and effective use of analgesics for acute musculoskeletal pain at home.
The focus is on acetaminophen, NSAIDs, and opioids.
|
Expérimental: Video plus Phone Follow-up
Patients will watch 10 minute educational video and receive phone call follow-up at 3 days to assess pain symptoms.
Patients with a pain score of 4 or more will receive another call with advice from a geriatric pain specialist.
|
This is a 10 minute interactive video which provided information to the viewer regarding the safe and effective use of analgesics for acute musculoskeletal pain at home.
The focus is on acetaminophen, NSAIDs, and opioids.
The call will be made by the study coordinator, who is a medical student.
Any patients reporting a pain score in the past 24 hours of 4 or more will be re-contacted by an emergency physician with special training in geriatric pain management.
This individual will provide recommendations to the patient regarding treatment options.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
Change in Pain Score
Délai: ED visit and 30 days post-ED visit
|
Change in Pain from emergency department (ED) visit to 30 day follow-up phone call will be measured by calculating the difference between the maximum pain score in the ED and the patient reported average overall pain severity in the past week using the 0-10 numeric rating scale for both measures.Change in pain will be reported as a negative number if the pain decreases (i.e., 10 to 8 = -2).
Higher scores indicate a worse outcome.
|
ED visit and 30 days post-ED visit
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
Number of Participants Experiencing Medication Side Effects
Délai: 30 days after ED visit
|
Patients were asked if they experienced any of the following side effects: fatigue, drowsiness, trouble sleeping, trouble thinking, dizziness, unsteadiness, nausea, vomiting, constipation, abdominal pain, black or bloody stool, trouble urinating, loss of appetite, itching or shortness of breath. Patients were also queried about any other side effects they had that were not on the list. Participants reporting at least one side effect were included. |
30 days after ED visit
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Average Overall Pain at One Month
Délai: 30 days after ED visit
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Determined using 0-10 numerical rating scale to answer the question "What is the average amount of pain you have experienced over the last week on a scale of 0-10.
where 0 means no pain and 10 means pain as severe as it could possibly be.
|
30 days after ED visit
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Mean Physical Function Scores
Délai: 30 days after ED visit
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Using a measure of higher-level physical function based on walking, climbing stairs, and carrying bags - scores range from 0 to 12 with higher score indicating higher function.
|
30 days after ED visit
|
Collaborateurs et enquêteurs
Les enquêteurs
- Chercheur principal: Tim Platts-Mills, MD, MSc, University of North Carolina, Chapel Hill
Publications et liens utiles
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
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 (Réel)
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
- 15-0986
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .
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