Effect of coping strategies training on the use of coping strategies and quality of life in adolescents with thalassemia major

Effect of coping strategies training on the use of coping strategies and quality of life in adolescents with thalassemia major the martyr Dastgheib Hospital, Shiraz 2012

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT2013112215484N1

Enrollment

Registered

2014-04-19

Start date

2013-03-10

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

Thalassemia. Major Thalassemia

Interventions

Intervention 1: Intervention group: training coping strategies for patients was conducted in the form of 6(90min) individual sessions, consisting of lectures and question and answer and…. One and two

Rehabilitation

Intervention group: training coping strategies for patients was conducted in the form of 6(90min) individual sessions, consisting of lectures and question and answer and…. One and two month after inte

Control group: routine care

Eligibility

Sex/Gender

All

Age

11 Years to 18 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: being 11-18 years old;presence of patient having Beta thalassemia major; necessity of blood transfusion; not suffering from chronic physical and mental illnesses according to information mentioned in patients case and physician diagnosis; complete satisfaction and Willingness of patients and their parents to participate in research; literacy of patients; Access to telephone to follow the training program by researcher; Participation in all of the training sessions; living with parents (nuclear family); not taking Yoga and acupuncture and other complementary medicine. Exclusion criteria: patients deaths; patients unwillingness to continue cooperation or discontinuation of them during research; diagnosis of another chronic physical or mental illness by physician during research or happeing any stressful events for patient and his/her family.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Coping Strategy. Timepoint: Before intervention, 1 month and 2 month after intervention. Method of measurement: Questionnaire.;Quality of life. Timepoint: Before intervention,1 month and 2 month after intervention. Method of measurement: Questionnaire.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Hashemi

Shiraz University of Medical Sciences

Hashemif@sums.ac.ir+98 71 1646 6560

Outcome results

None listed

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