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CompletedNCT07514468IntegrativeUpdated Apr 7, 2026

Effectiveness of Integrative Therapy on Psychological Hardiness Among Hard-of-Hearing Female Students

An interventional study of Integrative Therapeutic Program in Deaf, Hard of Hearing and Hearing Disability, sponsored by King Faisal University. Completed at 1 site in Saudi Arabia. Open to female participants aged 13 Years to 19 Years. Per ClinicalTrials.gov, last updated 2026-04-07.

Sponsored by King Faisal University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 3 months after the study started (first participant enrolled Dec 2025, registered Mar 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
25
Allocation
Not applicable
Ages
13 Years to 19 Years
Sex
Female
01

Study summary

The goal of this clinical trial (quasi-experimental study) is to learn whether an integrative therapeutic program can enhance psychological hardiness among hard-of-hearing (HOH) female students in Saudi Arabia (Al-Ahsa Governorate). The main questions it aims to answer are:

  1. What is the level of psychological hardiness among DHH female students in the Kingdom of Saudi Arabia?
  2. Are there statistically significant differences in the level of psychological hardiness among DHH female students attributable to the study variables (degree of hearing loss, grade level, hearing assistive device, communication method used, parents' hearing status, and type of educational environment attended)?
  3. Are there statistically significant differences at the level of (α = 0.05) between the mean scores of the experimental group on the psychological hardiness scale in the pre- and post-measurements?
  4. Are there statistically significant differences at the level of (α = 0.05) between the mean scores of the experimental and control groups on the post-measurement of the psychological hardiness scale?

Researchers will compare students who participate in the integrative therapeutic program (experimental group) with those who do not (control group) to see if the program leads to improved psychological hardiness.

Participants will:

Complete a psychological hardiness scale before and after the program Participate in the integrative therapeutic training sessions (experimental group only) Continue their regular educational activities without intervention (control group)

Read the detailed description

This study was conducted to evaluate the effectiveness of an integrative therapeutic program in enhancing psychological hardiness among hard-of-hearing (HOH) female students in inclusive educational settings in Al-Ahsa Governorate, Kingdom of Saudi Arabia. HOH students often face multiple psychological and social challenges that may negatively affect their adaptive functioning and overall well-being. Therefore, this study aimed to provide an evidence-based intervention to strengthen psychological resilience and improve coping capacities within this population.

A quasi-experimental design with a non-randomized experimental and control group structure was adopted. The study initially involved a broader sample of 69 deaf and hard-of-hearing (DHH) female students. All participants were assessed using a Psychological Hardiness Scale developed and validated by the researchers. Based on (pre-test) results, a purposive sample of 25 HOH students who demonstrated relatively low levels of psychological hardiness was selected to participate in the intervention phase.

The selected participants were divided into two groups: an experimental group (n = 15), which received the integrative therapeutic program, and a control group (n = 10), which did not receive any intervention during the study period. The intervention program was designed to enhance key dimensions of psychological hardiness, including commitment, control, and challenge, through structured therapeutic activities and training sessions tailored to the communication abilities and learning needs of HOH students.

All participants underwent pre-test and post-test assessments using the same psychological hardiness scale. The primary outcome measure was the change in psychological hardiness scores between pre-test and post-test evaluations. The effectiveness of the intervention was determined by comparing within-group changes (pre- vs. post-test) and between-group differences (experimental vs. control group). The higher the student's score on the scale, the greater the improvement in her level of psychological hardiness.

The independent variable in this study was the integrative therapeutic program, while the dependent variable was psychological hardiness. Although the study design aimed to control for confounding variables, several external factors may have influenced the outcomes, including parental support, teacher preparedness, peer interactions, and the broader educational and social environment.

The findings demonstrated statistically significant improvements in psychological hardiness among participants in the experimental group compared to the control group, indicating the effectiveness of the implemented program. These results support the integration of structured therapeutic interventions within educational support services for HOH students to enhance their psychological well-being and quality of life.

02

Conditions studied

  • Deaf
  • Hard of Hearing
  • Hearing Disability

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Keywords

  • Integrative therapeutic program
  • psychological hardiness
  • hearing impairment
  • hard-of-hearing middle school students
03

In context

Hearing Loss

796 studies on the registry are indexed under Hearing Loss; 193 are open to participants now.

This study's enrollment of 25 is below the median of 44 across 561 interventional studies indexed under Hearing Loss.

Browse Hearing Loss studies →

Lead sponsor

King Faisal University is the lead sponsor of 15 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
13 Years to 19 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

After administering the scale, a purposive sample of 25 HOH female students was selected to participate in the intervention program. These participants were divided into two groups: 15 students in the experimental group and 10 students in the control group. This selection was determined due to the sensitivity of the research topic and the practical difficulty of conducting the intervention with the entire target population.

Eligibility Criteria

Inclusion criteria

Inclusion Criteria:

  1. Female students with hearing impairment (Hard of Hearing, HOH)
  2. Enrollment in inclusive schools in Al-Ahsa Governorate, Saudi Arabia
  3. Within the targeted educational stage of the study
  4. Low scores on the Psychological Hardiness Scale at (pre-test)
  5. Ability to participate in and complete the intervention program
  6. Provision of

Exclusion criteria

Exclusion Criteria:

  1. Failure to provide
  2. Incomplete participation in (pre-test) or post-intervention (post-test) assessments
  3. Diagnosis of profound deafness that limits effective communication required for the intervention
  4. Male students (excluded due to logistical and cultural constraints related to intervention delivery)
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
25 participants (actual)

Study arms

  • Experimental
    Integrative Therapeutic Program Group

    Participants in this arm will receive an integrative therapeutic program designed to enhance psychological hardiness among hard-of-hearing female students. The program includes structured training sessions focusing on cognitive, emotional, and behavioral strategies to improve resilience, coping skills, and adaptation to psychological stress. Participants will attend scheduled sessions over 4 Weeks, and their psychological hardiness will be assessed before and after the intervention using a standardized scale.

    Other: Integrative Therapeutic Program

Interventions

  • OtherIntegrative Therapeutic Program

    The therapeutic program was developed based on the integrative therapy approach, which involves combining techniques and strategies derived from multiple therapeutic schools in accordance with the characteristics of the target population, without adhering to a single theoretical framework. The integrative approach draws on contemporary integrative perspectives that emphasize flexibility in intervention according to the needs of beneficiaries. The program was also grounded in the psychological hardiness theory developed by Suzanne Kobasa, which conceptualizes hardiness through three dimensions: commitment, control, and challenge. In addition, the program incorporated techniques drawn from several therapeutic approaches, including: (Cognitive Behavioral Therapy (CBT), Rational Emotive Behavioral Therapy (REBT), Mindfulness-Based Therapy, Group Therapy, Gratitude Therapy, Reality Therapy, Supportive spiritual techniques)

06

What researchers measure

Primary outcomes

  1. Psychological Hardiness Scale for deaf and hard of hearing

    The final version of the Psychological Hardiness Scale consisted of two sections. The first section included demographic items related to: (degree of hearing loss, grade level, type of hearing assistive device, preferred communication method, parents' hearing status, type of educational environment attended). The second section, which constitutes the main scale, consisted of 24 items distributed across three dimensions: commitment, control, and challenge. Each item was rated using a four-point Likert scale: (1 = Never, 2 = Rarely, 3 = Often, 4 = Always). Minimum value 1 Maximum value 4 Therefore, a student who scores higher on the scale will have a higher degree of psychological resilience.

    Time frame: 8 weeks

  2. Change in Psychological Hardiness Scores

    This outcome measures the change in psychological hardiness among hard-of-hearing female students using a validated psychological hardiness scale developed by the researchers. The assessment evaluates key dimensions such as commitment, control, and challenge before and after the intervention. Accordingly, the higher the student's score on the psychological resilience scale between the pre-test and post-test, the more effective the implemented program is considered to be.

    Time frame: 8 weeks

07

Study locations

1 site
  • Schools for the hearing impaired in Al-Ahsa
    Al Mubarraz, 31982, Saudi Arabia
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 7, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07514468
Lead sponsor
King Faisal University
Responsible party
Nourah Ibrahim Albash (ِِAssistant professor, King Faisal University) — Principal investigator
First posted
Apr 7, 2026
Start date
Dec 25, 2025
Primary completion
Feb 26, 2026
Completion
Mar 2, 2026
Last update
Apr 7, 2026

Study contacts

Nourah I Albash
principal investigator · King Faisal University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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