- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT03366805
A Patient Education Video Program for Post-Operative Recovery After Upper Extremity Surgery
A Standardized Patient Education Video Program for Improvement of Post-Operative Recovery After Outpatient Upper Extremity Surgery
Przegląd badań
Status
Warunki
Szczegółowy opis
Four hundred (400) adult patients undergoing elective outpatient, upper extremity, orthopedic surgeries will be recruited by the surgeon-investigators. Patients will be randomized to view one of two educational programs: 1) a 2-video series regarding post-operative pain management or 2) a video regarding wound care and activity.
These patients will be encouraged to review the video online in the week before surgery. An intake enrollment form will be completed by an investigator using demographic information available in the chart.
Participants in both arms will complete their Patient Education Study Diary daily, for 7 days following their surgery. There are two versions of this diary: the Wound Education Version asks patients to report daily pain mediation use. The Pain Education Version does not include this section as patients in the pain management arm of the study record this information in their Recovery Diary.
The patient will be contacted again by phone and/or mail 1 year after surgery (12-14 months) using the contact information available in EPIC to determine the self-reported prevalence of chronic pain and pain medication use.
Typ studiów
Zapisy (Rzeczywisty)
Faza
- Nie dotyczy
Kontakty i lokalizacje
Lokalizacje studiów
-
-
Virginia
-
Roanoke, Virginia, Stany Zjednoczone, 24014
- Institute for Orthopedics and Neurosciences
-
-
Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion Criteria:
- Adult patients planning elective outpatient orthopedic surgery procedures by a Carilion Clinic hand surgeon will be eligible for the study.
Exclusion Criteria:
- Patients unable or unwilling to provide informed consent
- Patients unable to unwilling to participate in the trial (poor English language skills, blindness, cognitively disadvantaged, poor literacy skills, other barriers to participation)
- Patients who are or suspect they may be pregnant.
- Patients for whom the medical provider, in his professional judgment, does not feel that the study protocol would be appropriate. (to be tracked)
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie podtrzymujące
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Pojedynczy
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
---|---|
Aktywny komparator: Wound Care Video
Wound Care Patient Education Video
|
Patient education video that were created in-house specifically for this project.
|
Eksperymentalny: Pain Management Video Group
Pain Management Patient Education Video
|
Patient education video that were created in-house specifically for this project.
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
---|---|---|
Quality of Recovery 15 Score
Ramy czasowe: 2 days after surgery
|
Score on the standardized Quality of Recovery 15 questionnaire How have you been feeling in the last 24 hours? (0 to 10, where 0= none of the time [poor] and 10=all of the time [excellent]) 0 1 2 3 4 5 6 7 8 9 10
|
2 days after surgery
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
---|---|---|
PROMIS
Ramy czasowe: 3 days after surgery
|
PROMIS short forms administered on POD 3 - (GI belly pain 5a, GI nausea and vomiting 4a, Pain Intensity 3a, Pain Interference 4a, Sleep Disturbance 4a, Cognitive Function 4a)
|
3 days after surgery
|
number of narcotic pills used
Ramy czasowe: 7 days after surgery
|
number of narcotic pills used
|
7 days after surgery
|
daily pain level
Ramy czasowe: 7 days after surgery
|
0-10 rating scale
|
7 days after surgery
|
patient-reported satisfaction and feeling of control - pain management
Ramy czasowe: 7 days after surgery
|
Today, I feel in control of my pain management.
|
7 days after surgery
|
patient-reported satisfaction and feeling of control- wound care
Ramy czasowe: 7 days after surgery
|
Today, I feel in confident about how I am caring for my wound.
|
7 days after surgery
|
patient-reported satisfaction and feeling of control - pain management satisfaction
Ramy czasowe: 7 days after surgery
|
Today, I would rate my satisfaction with my pain control as (circle)
|
7 days after surgery
|
number of pain-related calls/visits to a healthcare provider
Ramy czasowe: 7 days after surgery
|
patient-reported
|
7 days after surgery
|
use of non-narcotic adjunct pain relief medication and modalities
Ramy czasowe: 7 days after surgery
|
7 days after surgery
|
|
incidence of high risk activities - sedating medication polytherapy
Ramy czasowe: 7 days after surgery
|
combining narcotics with muscle relaxants/sedatives/alcohol, other sedating medications
|
7 days after surgery
|
incidence of high risk activities - NSAID polytherapy
Ramy czasowe: 7 days after surgery
|
combining prn NSAIDs with regularly dosed prescription NSAIDs
|
7 days after surgery
|
incidence of high risk activities - overdosing
Ramy czasowe: 7 days after surgery
|
exceeding daily recommended doses of pain medication
|
7 days after surgery
|
incidence of side effects and adverse events - Nausea/V omitting
Ramy czasowe: 7 days after surgery
|
Nausea/Vomiting
|
7 days after surgery
|
incidence of side effects and adverse events - Dizziness/balance problems
Ramy czasowe: 7 days after surgery
|
Dizziness/balance problems
|
7 days after surgery
|
incidence of side effects and adverse events - fatigue or sedation
Ramy czasowe: 7 days after surgery
|
fatigue or sedation
|
7 days after surgery
|
incidence of side effects and adverse events - headache
Ramy czasowe: 7 days after surgery
|
headache
|
7 days after surgery
|
incidence of side effects and adverse events - visual changes
Ramy czasowe: 7 days after surgery
|
visual changes
|
7 days after surgery
|
incidence of side effects and adverse events - stomach pain
Ramy czasowe: 7 days after surgery
|
stomach pain
|
7 days after surgery
|
incidence of side effects and adverse events - constipation
Ramy czasowe: 7 days after surgery
|
constipation
|
7 days after surgery
|
incidence of side effects and adverse events - diarrhea
Ramy czasowe: 7 days after surgery
|
diarrhea
|
7 days after surgery
|
incidence of side effects and adverse events - fever
Ramy czasowe: 7 days after surgery
|
fever
|
7 days after surgery
|
incidence of side effects and adverse events - rash
Ramy czasowe: 7 days after surgery
|
rash
|
7 days after surgery
|
incidence of side effects and adverse events - hives
Ramy czasowe: 7 days after surgery
|
hives
|
7 days after surgery
|
incidence of side effects and adverse events - swelling
Ramy czasowe: 7 days after surgery
|
swelling
|
7 days after surgery
|
incidence of side effects and adverse events - difficulty breathing/shortness of breath
Ramy czasowe: 7 days after surgery
|
difficulty breathing/shortness of breath
|
7 days after surgery
|
incidence of side effects and adverse events - heart palpitations/arrythmia/heart racing
Ramy czasowe: 7 days after surgery
|
heart palpitations/arrythmia/heart racing
|
7 days after surgery
|
incidence of side effects and adverse events - anaphylaxis
Ramy czasowe: 7 days after surgery
|
anaphylaxis
|
7 days after surgery
|
incidence of side effects and adverse events - ringing in ears
Ramy czasowe: 7 days after surgery
|
ringing in ears
|
7 days after surgery
|
incidence of side effects and adverse events - other
Ramy czasowe: 7 days after surgery
|
other
|
7 days after surgery
|
demonstrated patient knowledge
Ramy czasowe: 7 days after surgery
|
as measured by score on the follow-up quiz
|
7 days after surgery
|
prevalence of chronic opioid use
Ramy czasowe: 1 year after surgery
|
patient reported
|
1 year after surgery
|
Współpracownicy i badacze
Sponsor
Śledczy
- Główny śledczy: Cassandra Mierisch, MD, Carilion Clinic
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Oczekiwany)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- 2266
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .
Badania kliniczne na Wound Care Patient Education Video
-
Laboratoires URGONieznany
-
University of MichiganAgency for Healthcare Research and Quality (AHRQ)Zakończony
-
Huntleigh Healthcare LtdSerenaGroup, Inc.Zakończony
-
Imperial College Healthcare NHS TrustZakończonyBadanie piersiZjednoczone Królestwo