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Phase 2 N=12 Randomized Double-blind Treatment

Vet-Harts Pilot Intervention for Veterans With Coronary Heart Disease

Heart Disease

Enrolled (actual)
12
Serious AEs
0.0%
Results posted
Dec 2018
Primary outcome: Primary: SF-36v Physical Function Scale — -6.67; 13.33 units on a scale

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Motivational Interview (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
VA Office of Research and Development
Primary completion
Jun 2012

Outcome Measures

OutcomeResultp-value
PRIMARY
SF-36v Physical Function Scale
-6.67; 13.33
PRIMARY
SF-36v Role Limitations Due to Physical Health Scale
-22.92; 9.38
PRIMARY
SF-36v Role Limitations Due to Emotional Problems Scale
-27.78; 5.56
PRIMARY
SF-36v Energy-Fatigue Scale
-5.00; 1.67
PRIMARY
SF-36v Emotional Well-Being Scale
-14.67; -2.00
PRIMARY
SF-36v Social Functioning Scale
-16.67; -10.42
PRIMARY
SF-36v Pain Scale
-5.00; 14.17
PRIMARY
SF-36v General Health Scale
-5.00; 4.17
PRIMARY
Seattle Angina Questionnaire Physical Limitations Scale
-5.93; 3.33
PRIMARY
Seattle Angina Questionnaire Angina Stability Scale
25.00; -12.50
PRIMARY
Seattle Angina Questionnaire Angina Frequency Scale
20.00; 16.67
PRIMARY
Seattle Angina Questionnaire Treatment Satisfaction Scale
-3.92; 7.84
PRIMARY
Seattle Angina Questionnaire Disease Perception Scale
13.89; 9.72

Summary

The purpose of this research study is to survey patients to learn about their beliefs and behaviors related to the management of heart disease and to discuss options for making healthy lifestyle changes. From the information the investigators get from patients, the investigators hope to develop better methods for taking care of patients who have heart disease.

Eligibility Criteria

Inclusion Criteria

  • Admission to an inpatient medicine unit for MI, ACS, and coronary angiography
  • Age

Exclusion Criteria

  • Altered mental status
  • Language barriers
  • Dementia or Cognitive Impairment
  • Diagnostic Study
  • Resident in long-term care facility prior to the present admission
  • Planned discharge to a skilled or intermediate care facility or hospice
  • Lack of access to a functioning phone
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01566214). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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