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Effect of Unified Transdiagnostic Treatment (UP) and Roy's adaptation model in treatment of hypertensio

Not Applicable
Conditions
Hypertension.
Essential (primary) hypertension
Registration Number
IRCT20210717051911N1
Lead Sponsor
The University of Lorestan
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
60
Inclusion Criteria

Have a minimum score of 19 or higher on the stress subscale of the DASS-21 questionnaire
Being over 18 years old
Having the minimum physical and cognitive abilities necessary to participate in the interventions
Systolic blood pressure equal to or greater than 140 and diastolic blood pressure equal to or greater than 90 mm Hg
Have a history of at least six months of medication for high blood pressure treatment
Tendency to participate in treatment sessions

Exclusion Criteria

Participate in other psychological interventions
Having a history of mental illness and taking psychotropic drugs

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Psychological distress. Timepoint: Before intervention and 8 weeks after intervention. Method of measurement: Depression Anxiety and Stress Scale.;Alexithymia. Timepoint: Before intervention and 8 weeks after intervention. Method of measurement: Toronto Alexithymia Scale.;Diet Adherence. Timepoint: Before intervention, The middle of intervention and after intervention. Method of measurement: Diet information registration form.;The amount of blood pressure systolic. Timepoint: Before intervention, The middle of intervention and after intervention. Method of measurement: Digital sphygmomanometer.;The amount of blood pressure diastolic. Timepoint: Before intervention, The middle of intervention and after intervention. Method of measurement: Digital sphygmomanometer.
Secondary Outcome Measures
NameTimeMethod
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