- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT02167737
The Emergency Department Stopping Elderly Accidents, Deaths and Injuries Program (ED-STEADI)
"ED-STEADI:" The Emergency Department Stopping Elderly Accidents, Deaths and Injuries Program (A Pilot Study)
Studienübersicht
Status
Intervention / Behandlung
Detaillierte Beschreibung
This prospective, randomized controlled study will be conducted when there is a member of the research team available to consent patients at a Level I Trauma Center with approximately 90,000 annual ED visits across all age groups. Each potentially eligible patient will be identified by the research team and approached in the ED. Consented and enrolled patients will be assigned a study identification number and the enrollment documented by a member of the research team in the ED's electronic medical record after subjects are confirmed to meet inclusion and exclusion criteria. Subjects will be assigned randomly (by using a computer generated sequence) to either the control or intervention study arms.
Subjects in the control arm will have demographic data collected, a baseline Falls Efficacy Scale (FES) and Vulnerable Elders Survey (VES) screening completed and two STEADI Tool Kit mobility tests administered (the "TUG" [Timed Up and GO] and the 30-Second Chair Stand test). The FES and VES are validated surveys measuring fall concern and functional decline. The research team will advise them that they have a risk of falling as identified by inclusion criteria and that we are advising them to take action to prevent future falls. They will be given the brochure, "What YOU Can Do to Prevent Falls," that is standardized information recommended in the STEADI Tool Kit for Health Care Providers by the Centers for Disease Control (CDC).
Subjects in the active arm will also have demographic data collected, a baseline FES and VES screening completed, and two STEADI Tool Kit mobility tests administered (the "TUG" [Timed Up and GO] and the 30-Second Chair Stand test). Their risk of falling will be reviewed with them using a bedside decision aid indicating what they can do to decrease their risk. Particular attention will be given to personalizing their fall risk. The fall prevention management options will be presented in a value neutral fashion, along with the advantages and disadvantages of each option. They will have an opportunity to discuss what outcomes are the most important to them and choose the management options from the list provided that are the most valuable to them. Study and treatment team members will then work with this agreed upon selection to provide reliable intervention and outpatient follow up to improve the gains that can be realized in an integrated healthcare system. If the participant chooses to do their own home safety evaluation, they will be provided with a checklist to guide them in looking for hazards in their home and how to fix them. The patient will keep the original copy of their decision aid with their agreed-upon selected treatment options, and a copy of it will be placed in the subject's study file. All actions that are in response to the subject's selected plan (prescriptions, appointments, etc.) will also be documented in the study file.
Both groups will have phone follow-up at 6 weeks post ED visit, and then again at 3, 6, 9 and 12 months to collect self-reported data about goal completion and fall history. The last phone follow-up will include an exit FES and VES reassessment. All participants in both arms will have data collected about their inpatient and outpatient visits throughout the network during the study period to corroborate their self-report (e.g., occupational therapy, physical therapy visits, hospital admissions or ER visits for injuries related to a fall, etc.).
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
-
-
Pennsylvania
-
Bethlehem, Pennsylvania, Vereinigte Staaten, 18017
- Lehigh Valley Hospital, Emergency Medicine Research
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
Patients must:
- Be 65 years of age or older
- Be discharged home from the ED
- Be able to speak English.
- Be competent and able to give consent (not in critical condition, intoxicated or otherwise incapacitated)
- Have a mechanical fall risk as defined by one of the following:
Reports to have fallen in the last year Reports worrying about falling Admits they feel unsteady when standing or walking
Exclusion Criteria:
Patients must not:
- Be younger than 65 years old
- Be discharged from the ED to anywhere, but home (i.e., must not be discharged to family member's home, personal care facility, nursing home, group home, etc.)
- Be unable to speak English
- Be incompetent and unable to give consent (in critical condition, intoxicated or otherwise incapacitated)
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Verhütung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
---|---|
Experimental: Bedside Decision Aid Group
This arm will include study participants who are randomized to the group utilizing the bedside decision aid, which has hospital staff arrange fall-risk reduction interventions (e.g., home safety checks, exercise programs, vision checks, etc.).
|
This group will have an initial FES and VES screening completed in the ED, the TUG test and Chair 30-Second Stand test, and the participant's risk of falling evaluated using our Bedside Decision worksheets. A study team member explains what subjects can do to decrease their risk of falling and discuss what mobility goals are the most important to them. Participants will receive a follow-up telephone call approximately six weeks after their discharge from the ED to collect self-reported data about goal completion, and then at four additional times--three, six, nine and 12 months--over the course of a year to collect self-reported data such as fall history. |
Aktiver Komparator: Control Arm
Participants in the control/comparator arm will experience the same study procedures with the exception of not using the Bedside Decision Aid and instead being given the Centers for Disease Control (CDC) brochure, "What You Can Do to Prevent Falls," and arranging for their own fall prevention strategies.
|
This group will also have an initial FES and VES screening completed in the ED and the same two mobility tests (TUG and Chair 30-Second Stand). Study staff will advise subjects on how to take action to prevent falls and give them a brochure, "What YOU Can Do to Prevent Falls," from the CDC's "STEADI Tool Kit for Health Care Providers." Participants will receive a telephone call approximately six weeks after their discharge from the ED to collect self-reported data about goal completion, and then at four additional times--three, six, nine and 12 months--over the course of a year to collect self-reported data such as fall history. |
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
---|---|---|
Efficacy of the bedside decision tool/worksheet
Zeitfenster: 12 months
|
A single sheet bedside decision aid form/worksheet will be used to engage the patient in a discussion about fall prevention, the aim of which is to increase patient interest and participation in different management options that decrease fall risk.
Patients will be followed up via phone calls re: their management option choices and how thorough/successful they were in completing them.
|
12 months
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
---|---|---|
Gender differences in use of the decision tool
Zeitfenster: 12 months
|
Responses from the bedside decision tool choices will be grouped by gender to determine if men and women select different management options and/or have different patterns in completing them.
|
12 months
|
Andere Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
---|---|---|
Gender differences in fall management choices
Zeitfenster: 12 months
|
Participants in *both* study arms will have phone follow-ups at the same time intervals to determine if men and women have different management option preferences and/or different patterns in completing them.
|
12 months
|
Mitarbeiter und Ermittler
Sponsor
Ermittler
- Hauptermittler: Marna R. Greenberg, DO, MPH, Lehigh Valley Hospital
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- #PRO-00001450
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Beschreibung des IPD-Plans
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
Klinische Studien zur Versehentliche Stürze
-
National Taiwan University HospitalAbgeschlossen
-
University Hospital, Strasbourg, FranceNoch keine RekrutierungPost-Fall-Syndrom | Psychomotorisches DesadaptationssyndromFrankreich
-
University Hospital, ToulouseSafe Step and Walk Movement (SSWM), Toulouse, FranceAbgeschlossenPost-Fall-SyndromFrankreich
-
Reproductive Medicine Associates of New JerseyAbgeschlossenJeder Patient ist sowohl Fall als auch Kontrolle | 1 Embryo wird biopsiert und 1 Embryo nichtVereinigte Staaten
-
University Hospital, Clermont-FerrandBeendetKeratokonus in einem oder zwei Augen für den Fall | Gute Sehschärfe zur KontrolleFrankreich
-
Ain Shams Maternity HospitalUnbekanntFall-Kontroll-Studie
-
Fondation Ophtalmologique Adolphe de RothschildAbgeschlossenSchätzung der Prävalenz neurologischer und neurovaskulärer Manifestationen in der Bildgebung im Fall von SARS-CoV-2 mit dem Beitrag einer optimierten MRTFrankreich
-
Hospital Universitari Vall d'Hebron Research InstituteAbgeschlossen
-
University Hospital, LilleAbgeschlossenFall-Kontroll-Studie | Magenkrankheit | Siegelringzellkarzinom | Speiseröhre | PrognoseFrankreich
-
Vanderbilt University Medical CenterNational Institute of Neurological Disorders and Stroke (NINDS); National Institute...RekrutierungKognitive Dysfunktion | Alzheimer Erkrankung | Altern | Biomarker | Gehirn | Alter, 80 und älter | Fall-Kontroll-Studien | Neuropsychologische TestsVereinigte Staaten
Klinische Studien zur Bedside Decision Aid
-
NYU Langone HealthRekrutierung
-
Chinese University of Hong KongNoch keine RekrutierungScreening-KoloskopieHongkong
-
Children's Hospital Medical Center, CincinnatiAbgeschlossenColitis ulcerosa, KinderVereinigte Staaten
-
Hospital San Carlos, MadridFundacion Investigacion Interhospitalaria CardiovascularRekrutierungMyokardischämie | Koronare Herzkrankheit | Koronarer Vasospasmus | Mikrovaskuläre Angina | Chronisches KoronarsyndromSpanien
-
Chinese University of Hong KongAbgeschlossen
-
Temple UniversityNational Institute of Mental Health (NIMH)AbgeschlossenPsychotische StörungenVereinigte Staaten
-
Northwestern UniversityUniversity of California, Los Angeles; National Institute on Aging (NIA); University... und andere MitarbeiterAnmeldung auf EinladungPolypharmazieVereinigte Staaten
-
Guy's and St Thomas' NHS Foundation TrustRekrutierungIntubation; Schwierig oder FehlgeschlagenVereinigtes Königreich
-
Istituto Ortopedico GaleazziUniversity of MilanAbgeschlossen
-
Andrew Tomas ReisnerRekrutierungWunden und VerletzungenVereinigte Staaten