- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT01904838
The Healing Context in CAM: Instrument Development and Initial Validation - Calibration Study (HEAL2)
30 de novembro de 2015 atualizado por: Carol Greco, University of Pittsburgh
The Healing Context in Complementary and Alternative Medicine (CAM): Instrument Development and Initial Validation - Calibration 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 Calibration 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 who are receiving physical therapy, chiropractic care, 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.
Visão geral do estudo
Status
Concluído
Descrição detalhada
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.
Our 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 an item bank.
We 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 an item bank 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 year of this study, we expect to identify conceptual areas of potential importance to CAM interventions and patients, and identify and edit items to create an item bank assessing these conceptual areas.
Specific Aim 2: Calibrate items.
We 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 our Center for Integrative Medicine (CIM), and 3) 125 outpatients at a General Internal Medicine clinic.
During year 2-3 we administer the items in the item bank to the 1650 persons, conduct IRT and CTT analyses and refine the item bank to only those items that best assess the constructs.
Specific aim 2 will result in a Computerized Adaptive Testing (CAT) version of the HEAL, which maximizes information while minimizing patient time burden.
A static short form of the HEAL will be derived from the HEAL CAT in Aim 2. Specific Aim 3: Conduct initial validation studies.
We will evaluate convergent, discriminant, and predictive validity of the Healing Encounters and Attitudes List (HEAL) in a sample of chronic low back pain (CLBP) 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) or mindfulness-based stress reduction (MBSR) at the CIM, and 100 persons receiving conventional care (physical therapy) at Centers for Rehab Services referred by the General Internal Medicine Clinic (GIMC) of the University of Pittsburgh Medical Center (UPMC).
We 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 treatment outcome measures for CLBP of pain and disability.
• Hypothesis 3a: Scores on the HEAL measure will display moderate to large correlations (r's > .50)
with similar self-report measures, supporting convergent validity.
• Hypothesis 3b: Scores on the HEAL measure 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, we predict that HEAL scores will demonstrate incremental validity, i.e., they will account for significant incremental variance in outcome beyond that accounted for by existing measures of treatment expectancy and related constructs.
Tipo de estudo
Observacional
Inscrição (Real)
1650
Contactos e Locais
Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.
Locais de estudo
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Pennsylvania
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Pittsburgh, Pennsylvania, Estados Unidos, 15213
- University of Pittsburgh Medical Center
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Critérios de participação
Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.
Critérios de elegibilidade
Idades elegíveis para estudo
18 anos e mais velhos (Adulto, Adulto mais velho)
Aceita Voluntários Saudáveis
Não
Gêneros Elegíveis para o Estudo
Tudo
Método de amostragem
Amostra Não Probabilística
População do estudo
Local clincal sample is persons receiving treatment at UPMC clinics or UPMC Center for Integrative Medicine.
Internet sample is persons reporting current or past year conventional or integrative medicine treatment.
Descrição
Inclusion Criteria:
- 1. age 18 or over
- 2. Males and Females
- 3. able to read, speak and understand English
- 4. able to complete informed consent procedures
- 5. able to complete questionnaires on a computer
- 6. (local sample arm:) began treatment within the past 4 weeks at the UPMC Center for Integrative Medicine or conventional medical clinics at UPMC.
- 7. (internet sample arm) self report of current or past year integrative medicine or conventional medical treatment.
Exclusion Criteria:
- 1. self reported History of schizophrenia or current psychotic symptoms
- 2. self reported uncontrolled current bipolar disorder
- 3. self report of substance dependence within the past 6 months
- 4. self reported history of organic neuropsychiatric syndromes (e.g., Alzheimer's, Parkinson's, dementia)
- 5. Lack of willingness or ability to provide informed consent
Plano de estudo
Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.
Como o estudo é projetado?
Detalhes do projeto
Coortes e Intervenções
Grupo / Coorte |
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Patients in Pittsburgh, Pennsylvania
persons receiving treatment at integrative and conventional medicine clinics in Pittsburgh, Pennsylvania
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Internet sample
internet sample of persons reporting that they receive, or have received in the past year, integrative medicine or conventional medical treatments.
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
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Patient-reported perspectives on relationship with provider, treatment expectancy, attitudes towards healthcare
Prazo: Baseline (generally same day as enrollment, but may occur at a single study visit within 4 weeks of enrollment)
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Participants' opinions regarding factors that contribute to healing, such as important patient characteristics, provider characteristics, and environmental factors
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Baseline (generally same day as enrollment, but may occur at a single study visit within 4 weeks of enrollment)
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Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
Investigadores
- Investigador principal: Carol M Greco, Ph.D., University of Pittsburgh
Publicações e links úteis
A pessoa responsável por inserir informações sobre o estudo fornece voluntariamente essas publicações. Estes podem ser sobre qualquer coisa relacionada ao estudo.
Datas de registro do estudo
Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.
Datas Principais do Estudo
Início do estudo
1 de setembro de 2012
Conclusão Primária (Real)
1 de setembro de 2013
Conclusão do estudo (Real)
1 de novembro de 2014
Datas de inscrição no estudo
Enviado pela primeira vez
17 de julho de 2013
Enviado pela primeira vez que atendeu aos critérios de CQ
19 de julho de 2013
Primeira postagem (Estimativa)
22 de julho de 2013
Atualizações de registro de estudo
Última Atualização Postada (Estimativa)
2 de dezembro de 2015
Última atualização enviada que atendeu aos critérios de controle de qualidade
30 de novembro de 2015
Última verificação
1 de novembro de 2015
Mais Informações
Termos relacionados a este estudo
Outros números de identificação do estudo
- AT006453 -2
- R01AT006453 (Concessão/Contrato do NIH dos EUA)
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .