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Effect of telephone follow-up methods and group session on quality of life of patients with pacemaker in clinic Investment ,Chamran Hospital in Isfahan

Effect of telephone follow-up methods and group session on quality of life of patients with pacemaker in clinic Investment, Chamran Hospital in Isfahan

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT138805132289N1
Enrollment
65
Registered
2011-06-25
Start date
2007-07-25
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

Pacemaker Implatation. Surgical operation with implant of artificial internal device

Interventions

Intervention 1: For 20 patient in telephone follow up 12 phone calling were performed for 4 weeks, each call would last 20 min. Intervention 2: For 20 patient in group session group 4 group session we
Placebo
For 20 patient in telephone follow up 12 phone calling were performed for 4 weeks, each call would last 20 min.
For 20 patient in group session group 4 group session were performed one day a week, each session would last 20-40 min.
For 20 patient in control group the routine intervention(giving educational material) was done.

Sponsors

Isfahan University of Medical Science
Lead Sponsor
Isfahan University of Medical Science
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients are aged 18-80 years; are of both sexes; complete the individual consciousness, awareness of time, place and person possible Drmtalh companies have; For the first time pacemaker is embedded; Patients who have the ability to participate in the meetings are; have a telephone at home; mental disorder is not known in this field do not use drugs; speech and hearing problems are not known; during pregnancy and lactation not; surgery, while there is no pacemaker fitted; or physical mental disability which prevents the ability not participate in session. Exclusion criteria: patient's unwillingness to continue participating in the study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Quality of life. Timepoint: One month. Method of measurement: SF-36 questionaries.

Secondary

MeasureTime frame
Physical condition. Timepoint: one month. Method of measurement: AQOL questionaries.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAliakbari Fateme

Isfahan University of Medical Science

aliakbari@nm.mui.ac.iraliakbari@skums.ac.ir+98 38 1334 4912

Outcome results

None listed

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