Interpersonal Psychotherapy Online Training Study
Harnessing Technology for Training Clinicians to Deliver Interpersonal Psychotherapy
Interpersonal psychotherapy (IPT) is an evidence-based therapy for the treatment of eating disorders (including binge eating disorder, bulimia nervosa, and disordered eating not meeting full diagnostic criteria). On a basic level, IPT is a time-limited treatment that helps the client understand the relationship between symptoms and social interactions. Traditional training methods require substantial cost, time, and resources, making evidence-based treatments difficult to disseminate. As such, college clinicians are not typically trained in IPT delivery, which prevents their clients from reaping the potential benefits of treatment. This study will attempt to show how technology can overcome such barriers to training dissemination.
The purpose of this study is to see if online training in IPT is as effective as in-person training. To find out, the following procedures will occur: First, college mental health clinicians will complete baseline online questionnaires and deliver their usual treatment to 1 or 2 clients with symptoms of eating disorders. Then, they will complete the guided online training program and post-training assessments. Next, they will treat 1 or 2 different clients with eating disorders and complete post-training assessments. As part of the baseline and post-training assessments, clinicians will complete a telephone-based simulation assessment with staff raters, in which the investigators will recreate a client session and rate how well the clinicians adhere to IPT in treating the simulated client. The guided on-line training program will ultimately be compared to the "gold standard" training (the group receiving in-person training in an associated, IRB-approved study, # 201111113).
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Tipo de estudo
Inscrição (Real)
Estágio
- Não aplicável
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
THERAPISTS:
Inclusion criteria:
- Therapist must be a staff member at the counseling center and have a patient case-load large enough to be able to complete data collection at the different time points (>8 hours/week)
- Staff member is expected to continue working at the counseling center for several years • Postdocs who anticipate to be at their center for at least one year are eligible
Exclusion criteria:
- Therapists from all universities affiliated with the NIH-funded trial (IRB# 201111113)
- Therapists working less than 8 hours/week
- Therapists who are anticipating leaving employment at the recruited counseling center within the time frame of the study including, but not limited to trainees and interns
- Therapists for whom their administrative duties preclude seeing a sufficient number of clients to be able to complete data collection at the different study time points
- Therapists who do not see students seeking treatment for eating disorders
- Individuals who are non-degreed trainees (i.e., psychology interns)
STUDENTS:
Inclusion criteria:
- Student patients of therapists who seek counseling services at their respective schools
- Students exhibiting symptoms of an eating disorder
Exclusion criteria:
• Students exhibiting symptoms of anorexia nervosa
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: N / D
- Modelo Intervencional: Atribuição de grupo único
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: IPT Online Training
Therapists in this study will be trained in IPT using an online platform.
The program is self-paced but will have a deadline; the suggested pace is at least 12 hours spaced over 2 months.
The guided online training program was developed in collaboration with 3C institute, an award-winning research and development company that creates web- and evidence-based programs.
Content will be adapted from "gold-standard" training.
|
First, college mental health clinicians will complete baseline online questionnaires and deliver their usual treatment to 1 or 2 clients with symptoms of eating disorders.
Then, they will complete the guided online training program and post-training assessments.
Next, they will treat 1 or 2 different clients with eating disorders and complete post-training assessments.
As part of the baseline and post-training assessments, clinicians will complete a telephone-based simulation assessment with staff raters, in which the investigators will recreate a client session and rate how well the clinicians adhere to IPT in treating the simulated client.
The guided on-line training program will ultimately be compared to the "gold standard" training.
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Treatment fidelity: Adherence
Prazo: 1-3 years
|
Therapist's adherence to the procedures of IPT.
This will be assessed using the IPT Fidelity Assessment.
This scale was developed for the current study and was informed by work done by the Veterans' Health Administration, previous work conducted by the Principal Investigators of the current trial, and by other IPT researchers training therapists to conduct evidence-based treatments.
|
1-3 years
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Treatment fidelity: Competence
Prazo: 1-3 years
|
Therapist's level of competence in applying the procedures of IPT.
This will be assessed using the IPT Fidelity Assessment.
This scale was developed for the current study and was informed by work done by the Veterans' Health Administration, previous work conducted by the Principal Investigators of the current trial, and by other IPT researchers training therapists to conduct evidence-based treatments.
|
1-3 years
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Denise Wilfley, PhD, Scott Rudolph University Professor of Psychiatry, Medicine, Pediatrics, and Psychological & Brain Sciences, Washington University School of Medicine
- Diretor de estudo: Terry Wilson, PhD, Oscar K. Buros Professor of Psychology, Rutgers University
- Diretor de estudo: Stewart Agras, MD, Professor of Psychiatry (Emeritus), Stanford University, School of Medicine
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
Conclusão Primária (Real)
Conclusão do estudo (Real)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- 201408037
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Informações sobre medicamentos e dispositivos, documentos de estudo
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