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The effect of intervention based on health belief model on parent's anxiety, follow up examinations and velocity of retinal vascularization in retinopathy of prematurity

The effect of intervention based on health belief model on parent's anxiety, follow up examinations and velocity of retinal vascularization in retinopathy of prematurity

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200130046307N1
Enrollment
60
Registered
2020-02-08
Start date
2020-02-09
Completion date
Unknown
Last updated
2020-02-24

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

Conditions

Condition 1: retinopathy of prematurity. Condition 2: health belief model. Condition 3: Situational anxiety. retinopathy of prematurity health belief model Situational anxiety

Interventions

Intervention group: This randomized controlled clinical trial will be performed on at least 60 infants with premature retinopathy and their parents referring to ROP Clinic of Khatam Al Anbia Eye Hospi

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Parent Criteria for Inclusion: Having written consent to participate in the study, having read and write literacy. Test scores above 30 in the Spiel Berger Situational Anxiety Questionnaire. Inclusion criteria for neonates: Research unit infants with gestational age of 34 weeks (33 weeks and 6 days or less), infants weighing 2000 g or less, neonates with zone 2 and stage 2 retina screening examination.

Exclusion criteria

Exclusion criteria: Exclusion criteria for parents: unwillingness of the research unit to continue cooperating, having depression or anxiety disorder confirmed by a specialist physician during the study, participating in a similar training program during the study, more than one absenteeism session, history of maintenance An infant with retinopathy of prematurity, severe stressful events such as the death of first-degree relatives, divorces, or severe family disputes during the study. Exclusion criteria for neonates: neonatal death, clinical instability, and outpatient referral, such as hospitalization in the ICU, incidence of respiratory distress syndrome and need for mechanical ventilation during the study, severe asphyxia, and congenital major malformations

Design outcomes

Primary

MeasureTime frame
Parental Anxiety of Neonates with Retinopathy. Timepoint: Parental anxiety of neonates with retinopathy of prematurity, at baseline (before intervention), immediately after intervention. Method of measurement: Standard Spellberger questionnaire.;Parental adherence to the follow-up screening program for infants with retinopathy of prematurity. Timepoint: According to the schedule prescribed by the treating physician. Method of measurement: Form made by the researcher.;Velocity of retinal vascularization in retinopathy of prematurity. Timepoint: In accordance with Schedule of follow-up examinations in Retinopathy Executive Regulations. Method of measurement: Comparison of neonatal admission time to Posterior 2, Posterior 2, Anterior 2, Posterior 3 and Vascularization, respectively.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzam Salehnezhad

Mashhad University of Medical Sciences

salehnezhada2@mums.ac.ir+98 51 3270 4195

Outcome results

None listed

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