- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02356783
Implementation of Pedometer for Monitoring Step Count Pre and Post Lumbar ESI for Radicular Pain
Implementation of Wireless Pedometer for Monitoring Step Count Before and After Lumbar Epidural Steroid Injection for Radicular Pain.
Studieoversigt
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
-
-
New York
-
New York, New York, Forenede Stater, 10021
- Hospital For Special Surgery
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- 18 years of age and older
- Patients receiving lumbar epidural steroid injections as pain management to be scheduled at least one week away (-2 days/1 month).
- Patients who are able to understand how the Fitbit instrument works and are willing to consent to the study.
- Patient who used web-based communication frequently, e.g. Email.
- Patients who can speak, understand, and write in English.
- Prior MRI or an appointment to obtain an MRI prior to the procedure.
Exclusion Criteria:
- Workers' compensation cases.
- Patient does not have a computer at home.
- Non-ambulatory patients.
- Patients who have received a lumbar epidural steroid injection in the past 6 months.
- Nursing or pregnant women.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Støttende pleje
- Tildeling: Ikke-randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Andet: Interlaminar
Approach for lumbar epidural steroid injection for this arm will be interlaminar. We will be implementing a wireless pedometer to each of the 15 patients in this group to measure our primary and secondary outcomes. |
Wireless pedometer
|
|
Andet: Transforaminal
Approach for lumbar epidural steroid injection for this arm will be transforaminal. We will be implementing a wireless pedometer to each of the 15 patients in this group to measure our primary and secondary outcomes. |
Wireless pedometer
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Percentage of Patients With Available Step Count Data at Baseline.
Tidsramme: A week pre-procedure.
|
Percentage of patients with available step count data 7 days pre-procedure.
Step count will be obtained daily for 7 days using a wireless pedometer.
|
A week pre-procedure.
|
|
Percentage of Patients With Available Step Count Data Post-procedure.
Tidsramme: Duration of 60 days after procedure.
|
Percentage of patients with available step count data 60 days post-procedure.
Step count will be obtained using a wireless pedometer daily for a period of 60 days post-procedure.
|
Duration of 60 days after procedure.
|
Samarbejdspartnere og efterforskere
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Robert Griffin, MD, PhD, Hospital for Special Surgery, New York
Publikationer og nyttige links
Generelle publikationer
- Cohen SP, Bicket MC, Jamison D, Wilkinson I, Rathmell JP. Epidural steroids: a comprehensive, evidence-based review. Reg Anesth Pain Med. 2013 May-Jun;38(3):175-200. doi: 10.1097/AAP.0b013e31828ea086.
- MacVicar J, King W, Landers MH, Bogduk N. The effectiveness of lumbar transforaminal injection of steroids: a comprehensive review with systematic analysis of the published data. Pain Med. 2013 Jan;14(1):14-28. doi: 10.1111/j.1526-4637.2012.01508.x. Epub 2012 Oct 30.
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- #2014-135
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