- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02515552
Web-Based Program for Symptom Management in Fibromyalgia
3. august 2015 opdateret af: William Collinge, PhD, Collinge and Associates, Inc.
Fibromyalgia is a complex chronic illness affecting 6-12 million Americans.
Self-management strategies play a key role in reducing symptoms and maintaining functioning.
The proposed project offers a web-based self management tool that enables FM sufferers to identify significant linkages between their personal symptom levels and their personal self-management efforts over time in order to plan their own optimal approach to disease management.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
This Phase II project will complete development of the SMART (Self-Monitoring and Review Tool) Log program for symptom management and health promotion in FM and evaluate its efficacy in a large web-based trial that will closely emulate its planned application in Phase III.
The SMARTLog program is an interactive web-based self-monitoring and feedback intervention that employs proprietary statistical analysis procedures to give the user personally optimized guidance on behavioral, lifestyle and coping strategies that yield effective symptom reduction for that individual.
The program incorporates longitudinal collection and analysis of the individual's self-monitoring data followed by delivery of personalized feedback derived from those same personal data.
The program helps FM sufferers discover and monitor linkages between specific personal health-related behaviors and management strategies and their symptom levels over time.
Feasibility was demonstrated in Phase I by very high retention rates, ratings of satisfaction and perceived relevance, evidence of impact of utilization on improved well-being over the use period, and qualitative data indicating strong interest in continuation with the program.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
883
Fase
- Fase 2
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Oregon
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Eugene, Oregon, Forenede Stater, 97405
- Collinge and Associates, Inc.
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
21 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Self-reported presence of fibromyalgia
Exclusion Criteria:
- None
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Andet: All applicants
Study applicants who consented and completed the application to participate in the Fibromyalgia Wellness Project.
From that point forward all subjects used the intervention program to at whatever frequency they chose voluntarily.
It was recommended subjects complete a SMARTLog at least three times per week for at least three months.
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Web-based symptom and behavior self-monitoring program with automated feedback derived from the user's personal data.
A personal informatics approach is used involving proprietary within-subject statistical analysis procedures to determine user feedback that provides behavioral guidance based on statistically significant change in symptom levels associated with specific user behavior and self-management strategies.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Change in daily symptom Levels
Tidsramme: Baseline to user-defined end date (variable time series design) up to 9 months
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Change in Likert-scaled (0-10) daily symptom severity levels on the SMARTLog tracking instrument.
Daily reported levels over multiple days are aggregated to calculate trends over the user-defined reporting period.
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Baseline to user-defined end date (variable time series design) up to 9 months
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Sekundære resultatmål
Resultatmål |
Tidsramme |
---|---|
Change in Fibromyalgia Impact Questionnaire scores
Tidsramme: Baseline to user-defined end date (variable time series design) up to 9 months
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Baseline to user-defined end date (variable time series design) up to 9 months
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Change in Self-Efficacy for Chronic Disease Scale scores
Tidsramme: Baseline to user-defined end date (variable time series design) up to 9 months
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Baseline to user-defined end date (variable time series design) up to 9 months
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Change in SF12 scores
Tidsramme: Baseline to user-defined end date (variable time series design) up to 9 months
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Baseline to user-defined end date (variable time series design) up to 9 months
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Change in Multi-dimensional Health Locus of Control Scale scores
Tidsramme: Baseline to user-defined end date (variable time series design) up to 9 months
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Baseline to user-defined end date (variable time series design) up to 9 months
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Ledende efterforsker: William B Collinge, PhD, MPH, Collinge and Associates, Inc.
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Generelle publikationer
- Collinge W, Yarnold P, Soltysik R. Fibromyalgia Symptom Reduction by Online Behavioral Self-monitoring, Longitudinal Single Subject Analysis and Automated Delivery of Individualized Guidance. N Am J Med Sci. 2013 Sep;5(9):546-53. doi: 10.4103/1947-2714.118920.
- Collinge W, Soltysik R, Yarnold P. Fibromyalgia Impact Reduction Using Online Personal Health Informatics: Longitudinal Observational Study. J Med Internet Res. 2020 Apr 7;22(4):e15819. doi: 10.2196/15819.
Hjælpsomme links
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. september 2008
Primær færdiggørelse (Faktiske)
1. august 2011
Studieafslutning (Faktiske)
1. august 2011
Datoer for studieregistrering
Først indsendt
29. juli 2015
Først indsendt, der opfyldte QC-kriterier
3. august 2015
Først opslået (Skøn)
4. august 2015
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
4. august 2015
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
3. august 2015
Sidst verificeret
1. juli 2015
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- FM Wellness Project
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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