Transition From Hospital to Home Post Cardiac Condition
| Tracking Information | |||||
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| First Received Date ICMJE | June 23, 2011 | ||||
| Last Updated Date | April 18, 2013 | ||||
| Start Date ICMJE | August 2011 | ||||
| Primary Completion Date | December 2012 (final data collection date for primary outcome measure) | ||||
| Current Primary Outcome Measures ICMJE |
see primary outcome description below [ Time Frame: 2 years ] [ Designated as safety issue: No ] Of Aim 1 pts, 3 of 8 (37.5%) went to a follow-up appt w/in 2 weeks of discharge. Of Aim 3 pts, 6 of 7 (85.7%) had a follow-up w/in 2 weeks of discharge. Medication reconciliation was done w/in 2 weeks in 50% of Aim 1 pts and 100% of Aim 3 pts. Discharge summaries weren't available in the remote data for any of Aim 1 pts and all Aim 3 pts had discharge summaries sent to their PCPs prior to the follow-up appt. Routine discharge instructions were given to all Aim 1 pts at discharge. Teach-back discharge instructions were given to Aim 3 pts at discharge and follow-up phone calls. |
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| Original Primary Outcome Measures ICMJE |
Aim 3 -1) follow-up visit at primary care facility within 2-4 weeks of discharge; 2) medication reconciliation visit performed by pharmacist or PCP within 2-4 weeks of discharge; 3) hospitalization summary available to PCP prior to follow-up visit; 4) pa [ Time Frame: 2 years ] [ Designated as safety issue: No ] The proportion of patients receiving each process measures will be compared between patients enrolled in the initial interviews and in the pilot intervention to get a preliminary estimate of the impact of the intervention. The proportion of patients receiving each process of care measure will be described as proportions for categorical values and means with standard deviations for continuous variables. These preliminary comparisons provide estimates of effect size and inform sample size calculations for a larger study. |
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| Change History | Complete list of historical versions of study NCT01431846 on ClinicalTrials.gov Archive Site | ||||
| Current Secondary Outcome Measures ICMJE | Not Provided | ||||
| Original Secondary Outcome Measures ICMJE | Not Provided | ||||
| Current Other Outcome Measures ICMJE | Not Provided | ||||
| Original Other Outcome Measures ICMJE | Not Provided | ||||
| Descriptive Information | |||||
| Brief Title ICMJE | Transition From Hospital to Home Post Cardiac Condition | ||||
| Official Title ICMJE | Pilot Intervention to Improve the Transition From Hospital to Home | ||||
| Brief Summary | The study had three parts: Part 1: Patients (or their home caretakers) who live outside of Denver and receive their primary care at a location other than the Denver VAMC were interviewed after their discharge. The interview covered the patient's perspective about the transition of their medical care from the Denver VA to their primary care facility. Part 2: Primary care providers from the VA facilities that refer patients to the Denver VA were interviewed regarding their opinions of transition process from the Denver VA back to the primary care VA facilities. Part 3: The data from the above interviews were used to develop an intervention to improve the transition process from the Denver VA back to the primary care VA facilities. |
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| Detailed Description | Aim 1 was to describe barriers and facilitators of the transition process from hospital to home through qualitative interviews among patients discharged from Denver VA Medical Center (tertiary facility) after being transferred from a primary care VA. Aim 2 was to describe barriers and facilitators of the transition process through qualitative interviews among providers at primary care VA facilities who take care of patients discharged from the Denver VA Medical Center for a cardiac condition. Aim 3 was to pilot test the transitions of care intervention that targets patients and providers to evaluate the feasibility of the intervention to improve process of care measures, including: 1) PCP follow-up within 2-4 weeks of hospital discharge; 2) medications reconciled between pre and post-hospital discharge; 3) discharge summary available to PCP at time of visit; and 4) patient awareness of symptoms that require medical attention. This pilot was informed by the interviews from Aims 1 and 2 and best practices from the literature. Finally, as part of Aim 3, the primary care providers who saw the patients who completed the pilot were contacted to ask for their input and feedback regarding the pilot project. Description of Enrolled Population: Study Design and Research Methods This was a mixed methods study where both qualitative and quantitative methods were employed. Through a series of qualitative interviews (n=26), potential barriers and facilitators of the current discharge process were assessed in this hub and spoke model of cardiac care. Informed by these interviews, the transitions of care intervention refined elements from prior studies that have improved this transition process. Finally, a pilot test of this intervention was implemented to assess the effectiveness of the intervention to improve important processes of care during this transition period among patients (n=8) discharged from Denver VAMC after transfer from a primary care VA facility. |
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| Study Type ICMJE | Interventional | ||||
| Study Phase | Not Provided | ||||
| Study Design ICMJE | Allocation: Non-Randomized Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Health Services Research |
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| Condition ICMJE | Cardiac Condition | ||||
| Intervention ICMJE | Behavioral: Intervention
Informed by the interviews and best practices from the literature, pilot test the transitions of care intervention that targets patients and providers to evaluate the feasibility of the intervention to improve process of care measures, including: 1) PCP follow-up within 2-4 weeks of hospital discharge; 2) medications reconciled between pre and post-hospital discharge; 3) discharge summary available to PCP at time of visit; and 4) patient awareness of symptoms that require medical attention |
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| Study Arm (s) |
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| Publications * | Not Provided | ||||
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||
| Recruitment Status ICMJE | Completed | ||||
| Enrollment ICMJE | 34 | ||||
| Completion Date | December 2012 | ||||
| Primary Completion Date | December 2012 (final data collection date for primary outcome measure) | ||||
| Eligibility Criteria ICMJE | Inclusion Criteria: Aims 1 and 3:
Aim 2:
Exclusion Criteria: Aims 1 and 3:
Aim 2: There were exclusion criteria. |
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| Gender | Both | ||||
| Ages | 18 Years to 90 Years | ||||
| Accepts Healthy Volunteers | Yes | ||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
| Location Countries ICMJE | United States | ||||
| Administrative Information | |||||
| NCT Number ICMJE | NCT01431846 | ||||
| Other Study ID Numbers ICMJE | RRP 11-242 | ||||
| Has Data Monitoring Committee | No | ||||
| Responsible Party | Department of Veterans Affairs | ||||
| Study Sponsor ICMJE | Department of Veterans Affairs | ||||
| Collaborators ICMJE | Not Provided | ||||
| Investigators ICMJE |
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| Information Provided By | Department of Veterans Affairs | ||||
| Verification Date | February 2013 | ||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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