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Implementing Online Patient-Provider Communication Into Clinical Practice

Implementing Online Patient-Provider Communication Into Clinical Practice: Implementation Research

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00971139
Acronym
OPPC
Enrollment
199
Registered
2009-09-03
Start date
2009-11-30
Completion date
2013-12-31
Last updated
2015-11-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer, Diabetes, Injury of Liver

Keywords

Online patient-provider communication, Organizational change, Symptom management

Brief summary

This interdisciplinary, international collaboration study, including the the Norwegian Health Economy Administration (HELFO) will evaluate the effectiveness and real-world implementation of an online patient-provider communication (OPPC) service into rout ine practice. In Phase I we will identify patients and care providers requirements and organizational contexts, and use participatory design methods to adapt the OPPC service to users needs and the context of clinical practice. In Phase II we will offer study participants access to the OPPC service to understand implementation issues. In addition, we will conduct a pilot randomized clinical trial (usual care; OPPC) with 40 patients in each group that will be followed over 6 months.

Detailed description

A rapidly growing research literature documents the importance of Health IT to improve communication between health care providers and their patients. Patient Internet portals and online patient-provider communication (OPPC) allow patients to stay connected with their care providers between clinical encounters, get help and advice for their symptoms and problems from home, better understand and manage their illness, and become more engaged in their care. Through better patient-provider partnerships and communication independent of face-to-face visits, health problems and side-effects of treatment can be more easily detected, prevented, and treated more quickly. Therefore, the overall goal of this international collaboration study is to implement and evaluate the effects and use of a primarily nurse-administered OPPC service, including access to advice from physicians, dietitians and social counselors, as part of regular patient care; and using methods consistent with effectiveness research to bridge the gap between research evidence and translation into routine practice. The specific aims of this study are twofold: In Phase I the investigators will refine and implement an Internet-based OPPC service where patients can ask questions and receive advice and support from care providers and social counselors. The investigators will use participatory design methods to adapt an OPPC service to patients' needs; care providers' requirements; and the workflow and organizational and technical infrastructure of clinical practice by answering the following research questions: What are the predisposing, enabling and reinforcing factors related to successful adoption, implementation and maintenance of the OPPC service such as: potential barriers to successful implementation; workflow adjustments, support and resources needed to implement and maintain the OPPC in daily clinical practice? In Phase II we will offer study participants access to the OPPC service to understand implementation issues. In addition, we will conduct a pilot randomized clinical trial (usual care; OPPC) with 40 patients in each group that will be followed over 6 months to evaluate: 1. participation rate and OPPC use; 2. characteristics of high/low volume users, patient-caregiver communication and use patterns; 3. perceived usefulness and ease of use and 4. impacts on organizational change and interdisciplinary collaboration.

Interventions

BEHAVIORALAccess to an OPPC service

Access to an Internet-based messaging system where patients can ask questions and receive advice and support from care providers at the hospital and social counsellors

Sponsors

The Research Council of Norway
CollaboratorOTHER
Oslo University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 18 years of age. * Able to read/speak Norwegian and have Internet with secure access (BankID) at home.

Exclusion criteria

* Excluded are patients who have brain metastasis and patients with cerebral affection caused by the disease (e.g., encephalopathy) as this may affect their abilities to reliably report their symptoms. * Excluded are also patients who receive a liver transplant indicated by cancer coli, as they participate in another study.

Design outcomes

Primary

MeasureTime frame
Impacts of the OPPC service on organizational processes/organizational change such as care processesEnd of study at 6 (8) months after last included patient

Secondary

MeasureTime frame
Participation rate and OPPC use, perceived usefulness and ease of useEnd of study at 6 (8) months after last included patient
Characteristics of high/low volume users, patient-caregiver communication and use patternsEnd of study at 6 (8) months after last included patient

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026