NCT06392490

Brief Summary

The research was planned in a randomized controlled trial to evaluate the effect of technology-based education provided by peers and adults to children diagnosed with asthma in the 14-17 age group. The study will be conducted in two phases. The initial phase will assess the efficacy of the training provided to peer mentors. The subsequent phase will examine the impact of peer-led and adult-delivered technology-based education on quality of life, asthma control, asthma knowledge, and self-efficacy in adolescents diagnosed with asthma. The required institutional permission and ethics committee approval was received. The study group of the study will consist of 48 adolescents (intervention group 1 \[n=16\], intervention group 2 \[n=16\], and control group \[n=16\]). Data will be collected by using the descriptive features form, the Adolescent Asthma Self-Efficiacy Questionaire, the Asthma Quality of Life Scale for Children, the Asthma Control Test, the Asthma Knowledge Test.The data will be analyzed using the SPSS 27 program.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
48

participants targeted

Target at P25-P50 for not_applicable asthma

Timeline
Completed

Started Mar 2025

Shorter than P25 for not_applicable asthma

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 26, 2024

Completed
4 days until next milestone

First Posted

Study publicly available on registry

April 30, 2024

Completed
11 months until next milestone

Study Start

First participant enrolled

March 14, 2025

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 12, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 12, 2025

Completed
Last Updated

December 23, 2025

Status Verified

December 1, 2025

Enrollment Period

5 months

First QC Date

April 26, 2024

Last Update Submit

December 17, 2025

Conditions

Keywords

AsthmaAdolescentInformationEducationPediatricRandomized controlled trialQuality of lifeSelf-managementTechnologyInternetNursing

Outcome Measures

Primary Outcomes (4)

  • Adolescent Asthma Self-Efficacy Questionnaire

    The scale is applied to adolescents aged 12-18 with a diagnosis of asthma. Scale items are scored from 0 to 100. The responses to the scale items are added and then divided by 27 to obtain the total average score (0-100). Subscale items are added in the same way and divided by the number of items in each subscale. A higher score indicates higher self-efficacy.

    Change from Baseline level to 3 months (change is being assessed)

  • Asthma Quality of Life Scale for Children

    The instrument was developed to assess the physical, mental and social disorders of children diagnosed with asthma in the 7-17 age group. The scores range from 23 to 161. The items on the scale are evaluated using a 7-point Likert scale. A high score indicates a high quality of life, while a low score indicates a low quality of life.

    Change from Baseline level to 3 months (change is being assessed)

  • Asthma Control Test

    The Asthma Control Test (ACT) is a five-item instrument designed to assess asthma control. The ACT scores range from 5 to 25, with a score of 5 indicating poor asthma control and a score of 25 indicating complete control of asthma. A score below 19 is generally used to indicate uncontrolled asthma.

    Change from Baseline level to 3 months (change is being assessed)

  • Asthma knowledge test

    This form will be created by researchers in accordance with the existing literature. It will be used to evaluate information about asthma symptoms, triggers and treatment. The form will be created in a 3-point Likert type as "True", "False" and "I don't know". In the form, each correct answer will receive "1 point", while incorrect answers and those marked "I don't know" will receive "0 points". A high total score obtained from this form will indicate a high level of knowledge about asthma.

    Change from Baseline level to 3 months (change is being assessed)

Study Arms (3)

Peer Group

OTHER

-The experimental group that will apply the technology-based psychosocial program from peers

Other: Technology Based Asthma Program

Adult Group

OTHER

-The group that will apply the technology-based psychosocial program from adult

Other: Technology Based Asthma Program

Control Group

NO INTERVENTION

Control group that will no apply the technology-based psychosocial program

Interventions

Evaluate the impact of peer-led and adult-based technology-based education on the quality of life, asthma control, asthma knowledge and self-efficacy in adolescents diagnosed with asthma.

Adult GroupPeer Group

Eligibility Criteria

Age14 Years - 17 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)

You may qualify if:

  • the ages of 14 and 17 who have been diagnosed with asthma at least three months prior
  • who do not have any other medical diagnoses of chronic disease.
  • who must own and be able to use a smartphone, reliable home internet access, and a computer.
  • who must be proficient in Turkish and not be in the active attack period.
  • who must not have experienced a stressful event that could affect their quality of life in the last three months, such as an acute illness, the birth of a new sibling, or the death of a family member.

You may not qualify if:

  • who are unwilling or unable to continue the research
  • who fail to participate in the internet-based application on two or more occasions

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Emine Gunes San

Ankara, Turkey (Türkiye)

Location

MeSH Terms

Conditions

AsthmaAdolescent BehaviorChronic Disease

Condition Hierarchy (Ancestors)

Bronchial DiseasesRespiratory Tract DiseasesLung Diseases, ObstructiveLung DiseasesRespiratory HypersensitivityHypersensitivity, ImmediateHypersensitivityImmune System DiseasesBehaviorDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Phd candidate

Study Record Dates

First Submitted

April 26, 2024

First Posted

April 30, 2024

Study Start

March 14, 2025

Primary Completion

August 12, 2025

Study Completion

August 12, 2025

Last Updated

December 23, 2025

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share

There are no plans to make individual participant data (IPD) available to other researchers

Locations