FSU Hypertension Self-Care Training Study
| Status: | Active, not recruiting |
|---|---|
| Conditions: | High Blood Pressure (Hypertension) |
| Therapuetic Areas: | Cardiology / Vascular Diseases |
| Healthy: | No |
| Age Range: | 25 - Any |
| Updated: | 4/21/2016 |
| Start Date: | August 2012 |
| End Date: | June 2016 |
Improving the Willpower-based Self-care for Hypertension
The purpose of this study is to compare the effectiveness of two forms of self-care training
on the overall health of adults with hypertension.
on the overall health of adults with hypertension.
The FSU College of Social Work and the Department of Psychology are seeking adults age 25
and older with a clinical diagnosis of hypertension for a randomized trial using willpower
to manage high blood pressure. Voluntary participants will complete three phases: baseline,
intervention, and post-treatment. Baseline phase includes a preliminary phone screening,
fasting blood draw, physiological test (measuring heart rate variability, chest compression,
etc.), and a psychosocial inventory. Intervention phase includes 8 weeks of once weekly
trainings (approximately one hour long) to be held on a weekday evening. Participants will
be randomly assigned to one of the two willpower groups and will be asked to rehearse the
willpower method at least once daily for 30 minutes during these 8 weeks. Post-treatment
phase includes two follow-up booster sessions (at week 12 and week 16) for refreshing
willpower techniques, a follow-up fasting blood draw, a physiological test, and a
psychosocial inventory.
Participation is completely voluntary and confidential. Volunteers completing each of the
phases will be compensated $100 for their time. If someone is interested in participating,
they should call our office at 850-645-0247 or email fsuwillpower@gmail.com.
and older with a clinical diagnosis of hypertension for a randomized trial using willpower
to manage high blood pressure. Voluntary participants will complete three phases: baseline,
intervention, and post-treatment. Baseline phase includes a preliminary phone screening,
fasting blood draw, physiological test (measuring heart rate variability, chest compression,
etc.), and a psychosocial inventory. Intervention phase includes 8 weeks of once weekly
trainings (approximately one hour long) to be held on a weekday evening. Participants will
be randomly assigned to one of the two willpower groups and will be asked to rehearse the
willpower method at least once daily for 30 minutes during these 8 weeks. Post-treatment
phase includes two follow-up booster sessions (at week 12 and week 16) for refreshing
willpower techniques, a follow-up fasting blood draw, a physiological test, and a
psychosocial inventory.
Participation is completely voluntary and confidential. Volunteers completing each of the
phases will be compensated $100 for their time. If someone is interested in participating,
they should call our office at 850-645-0247 or email fsuwillpower@gmail.com.
Inclusion Criteria:
- Clinical diagnosis of hypertension
- Age 25 or older
Exclusion Criteria:
- Pregnancy
- Participation in other clinical trials or drug/behavioral treatment
- Previously participated in any other clinical trials/training on health-related
behavior (tai-chi, yoga, nutritional education, yoga class)
- Kidney disease
- Cancer/chemotherapy, advanced HIV/AIDS, severe liver disease
- Severe ischemic heart disease (unstable angina, hospitalization for heart attack,
coronary revascularization)
- Congestive heart failure
- Severe inflammatory/rheumatologic disorders (severe arthritis)
- Severe mental health diagnosis such as schizophrenia or bi-polar disorder
- Occurrence of any neurological disorders such as stroke or dementia
- Addicted to any legal/illegal drugs or alcohol without at least 1 year of sobriety
- Any infectious conditions such as pneumonia, traumatic wound, or surgery that may
cause inflammation in the past 14 days
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