The effect of sustained nursing consult by telephone (Tele Nursing) on blood pressure, quality of life and life style

The effect of sustained nursing consult by telephone (Tele Nursing) on blood pressure, quality of life and life style in hypertensive patients

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT2015062422903N1

Enrollment

Registered

2015-07-05

Start date

2013-12-22

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

High blood pressure. Essential (primary) hypertension

Interventions

Intervention 1: Intervention group: A consultation session with education at the beginning of study and then sustained nursing counseling by telephone during the 8 weeks. Intervention 2: Control group

Intervention group: A consultation session with education at the beginning of study and then sustained nursing counseling by telephone during the 8 weeks.

Control group: A consultation session with education at the beginning of study.

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria include: 6 month after diagnosis of hypertension; systolic blood pressure between 140-180 and diastolic blood pressure between 90-110 at the beginning of the study; ability to establish communication; don`t have any auditory or talking problem; accessibility to telephone; age range 18-65 years old Exclusion criteria include: Unwillingness to cooperate; Failure to Communicate by phone for more than 3 times; Developing dementia, mental and psychological problems; Hospitalization from any cause.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Blood pressure. Timepoint: At the beginning of the study (first step), after the 8 week intervention period (second step) and one month after the end of second step without any intervention in both groups (final step). Method of measurement: digital Sphygmomanometer.;Quality of life. Timepoint: At the beginning of the study (first step), after the 8 week intervention period (second step) and one month after the end of second step without any intervention in both groups (final step). Method of measurement: SF-36 questionaire.;Life style. Timepoint: At the beginning of the study (first step), after the 8 week intervention period (second step) and one month after the end of second step without any intervention in both groups (final step). Method of measurement: LSQ questionaire.	—

Measure

Time frame

Blood pressure. Timepoint: At the beginning of the study (first step), after the 8 week intervention period (second step) and one month after the end of second step without any intervention in both groups (final step). Method of measurement: digital Sphygmomanometer.;Quality of life. Timepoint: At the beginning of the study (first step), after the 8 week intervention period (second step) and one month after the end of second step without any intervention in both groups (final step). Method of measurement: SF-36 questionaire.;Life style. Timepoint: At the beginning of the study (first step), after the 8 week intervention period (second step) and one month after the end of second step without any intervention in both groups (final step). Method of measurement: LSQ questionaire.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactShahla Aliari

Aja University of Medical Sciences

sh.aliyari@ajaums.ac.ir+98 21 7750 0929

Outcome results

None listed

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