- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT02190240
Effect of Complementary and Alternative Medicine on Pain Among Inpatients
The proposed study has 3 aims: 1) quantitatively describe a model for delivering complementary and alternative medicine (CAM) therapies to understand the selection of patients and CAM therapies used for pain management, 2) examine the effects of selected CAM therapies on immediate change in pain, and 3) examine the effects of selected CAM therapies on duration of pain change.
Positive results from this study will assist hospitals in the integration of usual care and CAM therapy for pain reduction. Findings may also drive future research on the cost effectiveness of these therapies for pain management, as well as the impact on patient outcomes such as length of stay and use of narcotics.
Studieöversikt
Status
Betingelser
Studietyp
Inskrivning (Faktisk)
Kontakter och platser
Studieorter
-
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Minnesota
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Minneapolis, Minnesota, Förenta staterna, 55407
- Abbott Northwestern Hospital
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-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Testmetod
Studera befolkning
Beskrivning
Aims 1 and 2 Inclusion Criteria:
- Admission to Abbott Northwestern Hospital
- Consent to release of electronic health record for research purposes
- 18 years of age or older
- Length of stay greater than 24 hours
Aims 1 and 2 Exclusion Criteria:
- None
Aim 3 Inclusion Criteria:
- Admission to Abbott Northwestern Hospital
- Length of stay greater than 24 hours
- 18 years of age or older
- Consent to release of electronic health record for research purposes
- Received CAM therapy in current hospitalization
- Pain level of 1 or greater at the pre-treatment assessment by practitioner
- English-speaking
- Integrative medicine therapy ended between 9:00 am and 4:00 pm
Aim 3 Exclusion Criteria:
- Refuses consent
- Unable to provide consent due to competency concerns
- Has declined study participation 3 times during current hospitalization
- Has hard declined during current hospitalization
- Has been approached 6 times during current hospitalization
- Has been approached to consent earlier that day
Studieplan
Hur är studien utformad?
Designdetaljer
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Model of delivering CAM therapies
Tidsram: Up to 4 years
|
Quantitatively describe a model for delivering CAM therapies to understand selection of patients and CAM therapies used for pain management.
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Up to 4 years
|
|
Effects of selected CAM therapies on immediate change in pain
Tidsram: CAM Visit (30-45 minutes)
|
We will examine the effectiveness of CAM therapies on self-reported (11 point scale) pain measured just before and immediately after service delivery.
|
CAM Visit (30-45 minutes)
|
|
Effects of selected CAM therapies on duration of pain change.
Tidsram: 5 hours
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We will examine the effectiveness of CAM therapies on repeated measures of self-reported pain over several hours after therapy to assess the distribution and decay of the pain change effect.
|
5 hours
|
Samarbetspartners och utredare
Sponsor
Samarbetspartners
Utredare
- Huvudutredare: Jeffery Dusek, PhD, Allina Health
Publikationer och användbara länkar
Studieavstämningsdatum
Studera stora datum
Studiestart
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Uppskatta)
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Andra studie-ID-nummer
- AT006518-01
- R01AT006518-01 (U.S.S. NIH-anslag/kontrakt)
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