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Adherence to Palivizumab Prophylaxis

Primary Purpose

Congenital Heart Disease in Children, RSV

Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Phone call
Text message
Control
Sponsored by
Kosuyolu Heart Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Congenital Heart Disease in Children

Eligibility Criteria

1 Month - 24 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Diagnosis of congenital heart disease which are hemodynamically unstable, congestive heart failure, diagnosis of congenital heart disease with hemodynamically significant residual defects after corrective heart surgery, cardiomyopathy, pulmonary hypertension Being between 0-2 years of age Exclusion Criteria: Diagnosis of congenital heart disease in which palivizumab prophylaxis is not needed (the diagnosis of congenital heart diseases which are hemodinamically stable.) Becoming exitus during prophylaxis program Not being between 0-2 years of age

Sites / Locations

  • Kosuyolu Heart Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Status quo bias and implementation intention bias

Availability bias and social norm

Control

Arm Description

Participants' families in this arm were informed about prophylaxis program and provided a schedule additionally called two days before appointments (status quo bias) and were asked to plan the appointment day (implementation intention).

Participants' families in this arm were informed about prophylaxis program and provided a schedule and were received messages biweekly informing about benefits of program and adherence rate (availability bias and social norm).

Participants' families in this arm were informed about prophylaxis program and provided a schedule

Outcomes

Primary Outcome Measures

Effectiveness of cognitive biases in increasing adherence to prophylaxis programme
The average adherence rates in the control and treatment groups

Secondary Outcome Measures

The effect of father employment status (full-time, part-time, no) on the participants' adherence to the prophylaxis program
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
The effect of number of children in the family on the participants' adherence to the prophylaxis program
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
The effect of birth weight (weight in grams) on the participants' adherence to the prophylaxis program
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
The effect of number of intensive care unit admissions on the participants' adherence to the prophylaxis program
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
The effect of knowledge about respiratory syncytial virus previously (yes/no) on the participants' adherence to the prophylaxis program
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
The effect of finding prophylaxis program important or not (yes/no) on the participants' adherence to the prophylaxis program
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
The effect of the distance between home and hospital (km) on the participants' adherence to the prophylaxis program
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
The effect of number of difficulties about accessing to prophylaxis program on the participants' adherence to the prophylaxis program
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
The effect of family size (number of people living in the same house) on the participants' adherence to the prophylaxis program
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
The effect of the number of children in the school age on the participants' adherence to the prophylaxis program
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
The effect of family income (<1000 TL, 1000-2999 TL, 3000-4999 TL, 5000-6999 TL, 7000-8999 TL, >9000 TL ) on the participants' adherence to the prophylaxis program
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
The effect of smoking (yes/no) on the participants' adherence to the prophylaxis program
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
The effect of father and mother's age (years) on the participants' adherence to the prophylaxis program
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
The effect of father and mother education level (no education, primary school, high school, university) on the participants' adherence to the prophylaxis program
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
The effect of employment status of mother on the participants' adherence to the prophylaxis program
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
The effect of marital status (married, married- separated, divorced, widowed) on the participants' adherence to the prophylaxis program
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
The effect of health status of father and mother (in good health, in moderate health, in bad health) on the participants' adherence to the prophylaxis program
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.

Full Information

First Posted
February 17, 2023
Last Updated
March 18, 2023
Sponsor
Kosuyolu Heart Hospital
Collaborators
Sabanci University, Maras Necip Fazil City Hospital, Kirsehir Ahi Evran University, Van Research and Education Hospital, Sakarya University, Sivas Numune Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05778240
Brief Title
Adherence to Palivizumab Prophylaxis
Official Title
Behavioral Interventions to Increase Adherence to Palivizumab Prophylaxis in Children With Congenital Heart Disease: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Completed
Study Start Date
October 1, 2020 (Actual)
Primary Completion Date
December 31, 2020 (Actual)
Study Completion Date
June 1, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kosuyolu Heart Hospital
Collaborators
Sabanci University, Maras Necip Fazil City Hospital, Kirsehir Ahi Evran University, Van Research and Education Hospital, Sakarya University, Sivas Numune Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of this clinical trial is to analyze implications of two alternative nudge-interventions to increase adherence to palivizumab prophylaxis in children with congenital heart disease. The main questions investigators aim to answer are: Are well-established cognitive biases effective in increasing patient families' adherence to the palivizumab prophylaxis program? What are the factors that affect families' adherence to the prophylaxis program and whether and how the effects of interventions depend on these factors? To study these questions investigators planned to utilize four well-established cognitive biases in designing two alternative nudge-interventions and investigators measured the effectiveness of each nudge-intervention against a control group. Patients were randomly allocated to one control and two treatment groups. In the control group, investigators informed participants about the prophylaxis program and provided a schedule. Patients in the first treatment group were additionally called two days before appointments (status quo bias), and were asked to plan the appointment day (implementation intention). Patients in the second treatment group received biweekly messages informing them about the benefits of the program as well as the current adherence rate (availability bias and social norm).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Congenital Heart Disease in Children, RSV

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
229 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Status quo bias and implementation intention bias
Arm Type
Experimental
Arm Description
Participants' families in this arm were informed about prophylaxis program and provided a schedule additionally called two days before appointments (status quo bias) and were asked to plan the appointment day (implementation intention).
Arm Title
Availability bias and social norm
Arm Type
Experimental
Arm Description
Participants' families in this arm were informed about prophylaxis program and provided a schedule and were received messages biweekly informing about benefits of program and adherence rate (availability bias and social norm).
Arm Title
Control
Arm Type
Experimental
Arm Description
Participants' families in this arm were informed about prophylaxis program and provided a schedule
Intervention Type
Behavioral
Intervention Name(s)
Phone call
Intervention Description
Participants were given the vaccination appointment card and participants received a telephone call every month two days before their appointment. Participants were reminded that they have a set appointment and were asked to plan the day of their appointment as detailed below. The standard script used in the telephone call in every hospital was as follows:Hello, we are calling you because you are enrolled in the palivizumab prophylaxis research program. As you know, you have a vaccination appointment on [enter date] at [enter time]. To help you plan your day of appointment, we have a few short questions. At your appointment day, will you be coming to the hospital from home, or will you need to get permission from your workplace? What kind of transportation do you plan to take to come to the hospital at your appointment day? At what time do you plan to leave home or work to come to the hospital?
Intervention Type
Behavioral
Intervention Name(s)
Text message
Intervention Description
Participants were given the vaccination appointment card and participants were included in a messaging group (on Whatsapp or SMS, depending on the participant's preference) where, twice a month they received a message informing them on RSV, on the additional risks caused by RSV infection in children with congenital heart diseases and on the benefits of adherence to the prophylaxis program. These messages also involved statements about the high number of patient families that kept their appointments in the previous month.
Intervention Type
Behavioral
Intervention Name(s)
Control
Intervention Description
Participants were given the vaccination appointment card.
Primary Outcome Measure Information:
Title
Effectiveness of cognitive biases in increasing adherence to prophylaxis programme
Description
The average adherence rates in the control and treatment groups
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
The effect of father employment status (full-time, part-time, no) on the participants' adherence to the prophylaxis program
Description
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
Time Frame
8 weeks
Title
The effect of number of children in the family on the participants' adherence to the prophylaxis program
Description
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
Time Frame
8 weeks
Title
The effect of birth weight (weight in grams) on the participants' adherence to the prophylaxis program
Description
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
Time Frame
8 weeks
Title
The effect of number of intensive care unit admissions on the participants' adherence to the prophylaxis program
Description
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
Time Frame
8 weeks
Title
The effect of knowledge about respiratory syncytial virus previously (yes/no) on the participants' adherence to the prophylaxis program
Description
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
Time Frame
8 weeks
Title
The effect of finding prophylaxis program important or not (yes/no) on the participants' adherence to the prophylaxis program
Description
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
Time Frame
8 weeks
Title
The effect of the distance between home and hospital (km) on the participants' adherence to the prophylaxis program
Description
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
Time Frame
8 weeks
Title
The effect of number of difficulties about accessing to prophylaxis program on the participants' adherence to the prophylaxis program
Description
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
Time Frame
8 weeks
Title
The effect of family size (number of people living in the same house) on the participants' adherence to the prophylaxis program
Description
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
Time Frame
8 weeks
Title
The effect of the number of children in the school age on the participants' adherence to the prophylaxis program
Description
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
Time Frame
8 weeks
Title
The effect of family income (<1000 TL, 1000-2999 TL, 3000-4999 TL, 5000-6999 TL, 7000-8999 TL, >9000 TL ) on the participants' adherence to the prophylaxis program
Description
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
Time Frame
8 weeks
Title
The effect of smoking (yes/no) on the participants' adherence to the prophylaxis program
Description
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
Time Frame
8 weeks
Title
The effect of father and mother's age (years) on the participants' adherence to the prophylaxis program
Description
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
Time Frame
8 weeks
Title
The effect of father and mother education level (no education, primary school, high school, university) on the participants' adherence to the prophylaxis program
Description
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
Time Frame
8 weeks
Title
The effect of employment status of mother on the participants' adherence to the prophylaxis program
Description
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
Time Frame
8 weeks
Title
The effect of marital status (married, married- separated, divorced, widowed) on the participants' adherence to the prophylaxis program
Description
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
Time Frame
8 weeks
Title
The effect of health status of father and mother (in good health, in moderate health, in bad health) on the participants' adherence to the prophylaxis program
Description
Factor that affects participants' adherence to the prophylaxis program. The interaction of each factor on the treatment effect.
Time Frame
8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Month
Maximum Age & Unit of Time
24 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of congenital heart disease which are hemodynamically unstable, congestive heart failure, diagnosis of congenital heart disease with hemodynamically significant residual defects after corrective heart surgery, cardiomyopathy, pulmonary hypertension Being between 0-2 years of age Exclusion Criteria: Diagnosis of congenital heart disease in which palivizumab prophylaxis is not needed (the diagnosis of congenital heart diseases which are hemodinamically stable.) Becoming exitus during prophylaxis program Not being between 0-2 years of age
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elif Erolu, M.D.Ph.D.
Organizational Affiliation
Kosuyolu Heart Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kosuyolu Heart Hospital
City
Istanbul
Country
Turkey

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Adherence to Palivizumab Prophylaxis

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