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The effect of cooperation of treatment team and the patient on the quality of life in patients after coronary angioplasty

The effect of collaborative care on the quality of life of patients after coronary angioplasty

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015120120912N4
Enrollment
50
Registered
2016-03-03
Start date
2015-04-21
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

patients after coronary angioplasty. Presence of coronary angioplasty implant and graft

Interventions

Intervention 1: Intervention group: collaborative treatment program was conducted in 5 group sessions
in a way that 3 educational collaborative care sessions were conducted weekly and 2 collaborative care follow-up sessions were conducted every other week and each session was 45 to 60 minutes. At firs
Intervention group: collaborative treatment program was conducted in 5 group sessions
Control group: two group sessions were conducted to discuss the importance of medication, diet and exercise. sessions were held weekly each lasting 60 minutes.

Sponsors

Vice Chancellor for Research of Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: being aged more than 18 and less than 70 years; being conscious; having the ability to make communication; being aware of their disease; being able to read and write; not having an acute cardiovascular disease, diabetes type 1 and 2, hormone disorders and renal and mental diseases; having appropriate clinical condition according to physician’s diagnosis and not having any constraints for performing the interventions. Exclusion criteria: being absent for more than 2 educational sessions for intervention group; die or encounter any problem that would make them unable to continue the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Quality of life. Timepoint: Before the intervention and 3 month after intervention. Method of measurement: SF-36 questionnaire.

Secondary

MeasureTime frame
-. Timepoint: -. Method of measurement: -.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParastoo Rezapoor

Isfahan University of Medical Sciences

parastoo_rezapoor@yahoo.com+98 31 3792 2950

Outcome results

None listed

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