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

A Comparison of the Effectiveness of Unified Transdiagnostic Treatment (UP) and Application of Roy's adaptation model on Blood Pressure, Alexithymia, Psychological Distress and Diet Adherence in People with Hypertension Comorbid with Stress

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20210717051911N1

Enrollment

Registered

2021-08-14

Start date

2021-12-12

Completion date

Unknown

Last updated

2021-08-30

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

Conditions

Hypertension. Essential (primary) hypertension

Interventions

Intervention 1: The first intervention group: after taking part in a pre-test in a separate meeting, the participants will have the Unified Transdiagnostic treatment which includes 8 basic treatment f

2. Nursing diagnosis

3. Planning

4. Implementation

5. Assessment. In addition to the implementation of pre-tests, which is carried out on both the intervention and control group. In the intervention group, the first step is the evaluation and recognit

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

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

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

Design outcomes

Primary

Measure	Time frame
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.	—

Measure

Time frame

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.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarziyeh Kolivand

The University of Lorestan

marzikolivand@yahoo.com+98 66 4336 2078

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026