- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT02161887
The Healing Context in Complementary and Alternative Medicine (CAM): Initial Validation Study (HEAL)
28. února 2017 aktualizováno: Carol Greco, University of Pittsburgh
The Healing Context in CAM: Instrument Development and Initial Validation - Phase 3 Validation Study
The overall objective of this study is to develop and test an efficient set of self-report instruments to measure Complementary and Alternative Medicine(CAM)-relevant contextual factors important in healing.
The initial phase of the study involves developing and refining an item bank.
During the initial 'item bank development' phase, the investigators will run focus groups and cognitive interviews with individuals who participate in CAM and conventional medicine interventions.
The next step of instrument development is called Calibration, and involves administering the revised item bank to an internet sample and to persons who receive services in a CAM clinic and a conventional primary care setting.
The items will be calibrated using item response theory and classical test theory.
This will result in a computerized adaptive testing version of the instrument, as well as a static short form of the instrument.
This current protocol in ClinicalTrials.gov
pertains only to the final, Validation Phase of the study.
The final phase of the project will involve conducting initial validation studies of the set of instruments.
The set of instruments will be called the Healing Encounters and Attitudes Lists (HEAL).
The investigators will evaluate the convergent, discriminant, and predictive validity of the HEAL instruments in a sample of 200 persons with chronic low back pain or neck pain who are receiving physical therapy, chiropractic care, acupuncture, medical management, or mindfulness-based stress reduction.
For convergent validity, the HEAL is expected to display moderate to large correlations with measures of similar constructs.
The HEAL is expected to correlate modestly with self-report measures of general psychosocial functioning, in support of discriminant validity.
Finally, HEAL scores should account for a significant proportion of the variance in treatment outcome, supporting predictive validity.
Přehled studie
Postavení
Dokončeno
Detailní popis
This project will develop and test a set of patient self-report measurement tools to assess the perceived contextual factors, such as patient attitudes and expectations, patient provider relationship factors, and environmental factors that contribute to healing.
This project is synergistic with the National Institutes of Health (NIH) Roadmap initiative, Patient Reported Outcomes Measurement Information System (PROMIS), and will use the rigorous instrument development and validation methodology of PROMIS.
The overall objective of this study is to develop efficient self-report instruments to measure CAM-relevant contextual factors important in healing, hereafter referred to as the Healing Encounters and Attitudes Lists (HEAL), and conduct initial validation in persons seeking CAM and conventional treatment for pain.
Specific Aim 1: Develop item banks.
The investigators will employ several iterative steps used successfully in PROMIS to identify items that assess contextual factors of healing relevant to CAM.
Initial steps in developing item banks include: a) compilation and evaluation of existing instruments and relevant questions, b) consultation with experts, and c) focus groups with individuals who participate in CAM and conventional medicine interventions, and d) item editing.
During the initial phase of this study, the investigators expect to identify conceptual areas of potential importance to CAM interventions and patients, and identify and edit items to create item banks assessing these conceptual areas.
Specific Aim 2: Calibrate items.
The investigators will use item response theory (IRT) and classical test theory (CTT) to calibrate the items from Aim 1 on three samples: 1) an internet-based sample (n= 1400), 2) 125 outpatients participating in CAM interventions at the Center for Integrative Medicine (CIM), and 3) 125 outpatients at a General Internal Medicine clinic.
During year 3-4 the investigators will administer the items in the item banks to the 1650 persons, conduct IRT and CTT analyses and refine the item banks to only those items that best assess the constructs.
Specific aim 2 will result in Computerized Adaptive Testing (CAT) versions of the HEAL, which maximizes information while minimizing patient time burden.
Static short forms of the HEAL item banks will be derived from the HEAL CATs in Aim 2. Specific Aim 3: Conduct initial validation studies.
The investigators will evaluate convergent, discriminant, and predictive validity of the Healing Encounters and Attitudes List (HEAL) in a sample of chronic low back pain (CLBP) or neck pain patients receiving CAM and conventional medicine treatments.
The validity studies will use two samples of adults with CLBP: 100 persons receiving CAM treatments: chiropractic manipulation (CM), acupuncture, or mindfulness-based stress reduction (MBSR) at the CIM, and 100 persons receiving conventional care (physical therapy or medical management) at the University of Pittsburgh Medical Center (UPMC).
The investigators will administer the CAT version of the HEAL questionnaire developed in aims 1 and 2 as well as conventional measures of treatment expectancy, confidence in treatment provider, psychosocial functioning, and pain and disability treatment outcome measures for CLBP and neck pain.
• Hypothesis 3a: Scores on the HEAL measures will display moderate to large correlations (r's > .50)
with similar self-report measures, supporting convergent validity.
• Hypothesis 3b: Scores on the HEAL measures will correlate modestly (r's = .20-.35) with self-report measures of general psychosocial functioning, supporting discriminant validity.
• Hypothesis 3c: HEAL scores will account for a significant proportion of variance in treatment outcome in both samples.
In addition, the investigators predict that HEAL scores will demonstrate incremental validity, i.e., the scores will account for significant incremental variance in outcome beyond that accounted for by existing measures of treatment expectancy and related constructs.
Typ studie
Pozorovací
Zápis (Aktuální)
207
Kontakty a umístění
Tato část poskytuje kontaktní údaje pro ty, kteří studii provádějí, a informace o tom, kde se tato studie provádí.
Studijní místa
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Pennsylvania
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Pittsburgh, Pennsylvania, Spojené státy, 15213
- University of Pittsburgh Medical Center
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Pittsburgh, Pennsylvania, Spojené státy, 15232
- UPMC Shadyside Center for Integrative Medicine
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Pittsburgh, Pennsylvania, Spojené státy, 15213
- UPMC General Clinical Research Center
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Kritéria účasti
Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.
Kritéria způsobilosti
Věk způsobilý ke studiu
18 let a starší (Dospělý, Starší dospělý)
Přijímá zdravé dobrovolníky
Ne
Pohlaví způsobilá ke studiu
Všechno
Metoda odběru vzorků
Vzorek nepravděpodobnosti
Studijní populace
Patients who are beginning or about to begin CAM or Conventional Medicine treatments for chronic back pain or chronic neck pain in Pittsburgh, Pennsylvania at University of Pittsburgh Medical Center (UPMC).
Popis
Inclusion Criteria:
- 18 years old or older; able to read and understand English; able to use a computer; starting a new treatment for back or neck pain, or started treatment within the past month.
Exclusion Criteria:
- psychotic disorders.
Studijní plán
Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.
Jak je studie koncipována?
Detaily designu
Kohorty a intervence
Skupina / kohorta |
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Complementary Medicine Group
Patients receiving chiropractic care, acupuncture, or meditation for chronic pain
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Conventional Medicine Group
Patients receiving conventional medicine care (physical therapy, medication management) for chronic pain.
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Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Časové okno |
|---|---|
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Clinical Global Impression of Change (CGI)
Časové okno: 6 - 8 weeks, 4 months post study entry
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6 - 8 weeks, 4 months post study entry
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Sekundární výstupní opatření
Měření výsledku |
Časové okno |
|---|---|
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Roland and Morris Disability Questionnaire
Časové okno: Baseline, 6-8 weeks, 4 months post baseline
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Baseline, 6-8 weeks, 4 months post baseline
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Další výstupní opatření
Měření výsledku |
Časové okno |
|---|---|
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Neck Disability Index
Časové okno: Baseline, 6-8 weeks, 4 months post baseline
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Baseline, 6-8 weeks, 4 months post baseline
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Spolupracovníci a vyšetřovatelé
Zde najdete lidi a organizace zapojené do této studie.
Sponzor
Vyšetřovatelé
- Vrchní vyšetřovatel: Carol M Greco, Ph.D., University of Pittsburgh
Publikace a užitečné odkazy
Osoba odpovědná za zadávání informací o studiu tyto publikace poskytuje dobrovolně. Mohou se týkat čehokoli, co souvisí se studiem.
Obecné publikace
- Greco CM, Glick RM, Morone NE, Schneider MJ. Addressing the "It Is Just Placebo" Pitfall in CAM: Methodology of a Project to Develop Patient-Reported Measures of Nonspecific Factors in Healing. Evid Based Complement Alternat Med. 2013;2013:613797. doi: 10.1155/2013/613797. Epub 2013 Dec 19.
- Greco CM, Yu L, Johnston KL, Dodds NE, Morone NE, Glick RM, Schneider MJ, Klem ML, McFarland CE, Lawrence S, Colditz J, Maihoefer CC, Jonas WB, Ryan ND, Pilkonis PA. Measuring nonspecific factors in treatment: item banks that assess the healthcare experience and attitudes from the patient's perspective. Qual Life Res. 2016 Jul;25(7):1625-34. doi: 10.1007/s11136-015-1178-1. Epub 2015 Nov 12.
Termíny studijních záznamů
Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.
Hlavní termíny studia
Začátek studia
1. června 2014
Primární dokončení (Aktuální)
1. prosince 2016
Dokončení studie (Aktuální)
1. prosince 2016
Termíny zápisu do studia
První předloženo
10. června 2014
První předloženo, které splnilo kritéria kontroly kvality
11. června 2014
První zveřejněno (Odhad)
12. června 2014
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
3. března 2017
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
28. února 2017
Naposledy ověřeno
1. února 2017
Více informací
Termíny související s touto studií
Další relevantní podmínky MeSH
Další identifikační čísla studie
- AT006453-3
Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .
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