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AzTrials

Insomnia DisorderICBT-INCT07431034

Internet-Based Cognitive Behavioral Therapy for Insomnia in Persian-Speaking Adults

A study testing Omid Internet-Based CBT-I Program in people with Insomnia Disorder and Chronic Insomnia, run by Rasool Hamidi Choolabi at 1 site in Iran.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This study will test whether an internet-based cognitive behavioral therapy for insomnia (ICBT-I) delivered through the Persian-language web program "Omid" can improve sleep in Persian-speaking adults with insomnia. Read more about this study

Who is it for?
Ages 18 to 60 years
Conditions the study is for
Insomnia Disorder, Chronic Insomnia
What is being tested?
Omid Internet-Based CBT-I Program
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteIran
Study dates
21 Feb 2026to 4 May 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 60 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Age between 18 and 60 years.
  • Meets diagnostic criteria for insomnia disorder according to DSM-5, based on clinical interview or a validated screening procedure.
  • Insomnia Severity Index (ISI) score ≥ 10, indicating at least subthreshold insomnia.
  • Reports difficulty initiating or maintaining sleep or early-morning awakenings at least three nights per week for at least three months, with associated daytime impairment (e.g., fatigue, concentration problems, irritability).
  • Able to read and understand Persian.
  • Has regular access to the internet and a smartphone and/or computer to use the Omid web-based program.
  • Willing and able to provide informed consent and to complete online questionnaires and daily sleep diaries.

Who cannot join

  • Uncontrolled medical or neurological conditions that significantly interfere with sleep or require immediate treatment (e.g., untreated moderate-to-severe obstructive sleep apnea, uncontrolled epilepsy, unstable cardiac disease, advanced cancer).
  • Current shift work or rotating work schedules that regularly disrupt nighttime sleep.
  • Pregnancy.
  • Participation in another clinical trial or research study that could affect sleep during the study period.
  • Ongoing structured psychotherapy specifically targeting insomnia or other major psychiatric conditions within the past 6 months.
  • Current major depressive disorder or other severe psychiatric disorder (e.g., bipolar disorder, schizophrenia, psychotic disorders), as determined by clinical assessment or structured interview.
Show all 10Show fewer
  • Evidence of problematic substance use, such as heavy alcohol use (more than approximately 3 standard drinks per day on most days of the month) or frequent misuse of recreational drugs (e.g., cannabis use more than once per week), in the judgment of the investigators.
  • Active suicidal ideation or behavior requiring urgent clinical intervention.
  • Primary diagnosis of another untreated sleep disorder (e.g., restless legs syndrome, narcolepsy, circadian rhythm sleep-wake disorder) where insomnia is not the main problem.
  • Having an infant or child under 2 years of age whose care regularly disrupts nighttime sleep, in the judgment of the investigators.

Trial locations and contacts

1 site in 1 country.

Iran1 site
  • Shahid Beheshti University of Medical Sciences

    Tehran

Other trials in Iran

About this study

Official title: Evaluation of the Effectiveness of an Internet-Based Cognitive Behavioral Intervention on Sleep Quality, Insomnia Severity, and Daytime Sleepiness in Persian-Speaking Adults With Insomnia

This study will test whether an internet-based cognitive behavioral therapy for insomnia (ICBT-I) delivered through the Persian-language web program "Omid" can improve sleep in Persian-speaking adults with insomnia. Participants will be adults who have problems falling or staying asleep and meet diagnostic criteria for insomnia. Those who are eligible will be randomly assigned to either receive access to the Omid web-based CBT-I program or to a wait-list control group that will receive usual care during the study period. The Omid program provides weekly online modules with educational videos and texts about sleep and insomnia, sleep hygiene, stimulus control, sleep restriction, and cognitive techniques to manage unhelpful thoughts about sleep. Participants will complete questionnaires about insomnia severity, sleep quality, and daytime sleepiness before starting the program, after finishing the intervention, and at follow-up. The main goal is to see whether the Omid ICBT-I program reduces insomnia symptoms and improves overall sleep quality compared with the wait-list control group.

Read the detailed description

Insomnia is a common sleep disorder that can lead to impaired daytime functioning, reduced quality of life, and increased risk of physical and mental health problems. Cognitive behavioral therapy for insomnia (CBT-I) is recommended as a first-line treatment, but access to trained therapists and face-to-face services is often limited. Internet-based CBT-I programs may help to overcome these barriers by providing structured, evidence-based treatment remotely and at lower cost.

This randomized controlled trial will evaluate the effectiveness of "Omid," a Persian-language, internet-based CBT-I program for Persian-speaking adults with insomnia. The trial will use a parallel-group design with two arms: an intervention arm receiving Omid ICBT-I and a wait-list control arm receiving usual care during the study period. Adults aged 18 to 60 years who meet diagnostic criteria for insomnia disorder, can read and write Persian, and have access to the internet via a computer or smartphone will be recruited. Individuals with moderate to severe depression or anxiety, other untreated sleep disorders (such as sleep apnea or restless legs syndrome), substance abuse, or serious neurological or medical conditions will be excluded.

The Omid intervention consists of six weekly web-based sessions that participants are encouraged to complete at a pace of one session per week. Each session combines brief psychoeducational videos and reading materials, interactive exercises, and daily sleep diary completion. Session content covers introduction to insomnia and the CBT-I model, sleep hygiene, stimulus control, sleep restriction and adjustment of time in bed, management of worry and rumination, identification and modification of dysfunctional beliefs about sleep, review of progress, and relapse prevention planning. An optional "Calm Mind" module provides guided relaxation and mindfulness audio tracks, neutral bedtime stories, and soothing environmental sounds to help reduce pre-sleep arousal. The platform also offers additional written psychoeducational materials to deepen understanding of insomnia and CBT-I techniques. Adherence is supported through daily and weekly homework tasks, automated reminders via SMS or email, and simple visual feedback on sleep diary completion and progress through the program. The intervention is primarily self-guided, with limited therapist contact available for brief clarification and adherence support when needed.

Eligible participants will complete baseline assessments and then be randomly assigned, using permuted block randomization with varying block sizes, in a 1:1 ratio to either the Omid ICBT-I group or the wait-list control group. Allocation concealment will be ensured using sequentially numbered, opaque, sealed envelopes. The study is open-label; however, the allocation sequence will be concealed from those enrolling participants until assignment.

Participants in the Omid ICBT-I group will receive access to the Omid web platform for a fixed intervention period. The program delivers weekly online modules that include educational videos and texts about sleep and insomnia, sleep hygiene recommendations, stimulus control strategies (for example, using the bed only for sleep and getting out of bed when unable to sleep), sleep restriction instructions to consolidate sleep, and cognitive techniques to identify and modify unhelpful beliefs and worries about sleep. The platform also provides homework exercises and self-monitoring tasks designed to support behavior change and adherence to the new sleep schedule. Participants in the wait-list control group will receive usual care during the study and will be offered access to the Omid program after completion of the final follow-up assessments.

Outcome measures will be collected at baseline (before randomization), immediately after the intervention period, and at follow-up. The primary outcomes are insomnia severity, sleep quality, and daytime sleepiness, assessed using the Insomnia Severity Index (ISI), the Pittsburgh Sleep Quality Index (PSQI), and the Epworth Sleepiness Scale (ESS), respectively. The main hypothesis is that participants assigned to the Omid ICBT-I program will show greater reductions in insomnia severity and improvements in sleep quality and daytime sleepiness compared with the wait-list control group at post-intervention and follow-up. The results of this study will provide evidence on the effectiveness of a culturally adapted, Persian-language internet-based CBT-I program for adults with insomnia.

Being tested
Omid Internet-Based CBT-I Program
Keywords
Insomnia, Sleep Disorders, Cognitive Behavioral Therapy for Insomnia, CBT-I, Internet-based Intervention, Digital Therapeutics, Web-based CBT, Persian-speaking Adults, Omid Program
Medical subject headings
Sleep Initiation and Maintenance Disorders, Sleep Wake Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Omid Internet-Based CBT-I ProgramBehavioural

    Omid is a Persian-language, semi-guided, web-based cognitive behavioral therapy for insomnia (ICBT-I) program designed for Persian-speaking adults with insomnia. The program is delivered via a secure web platform accessible on computers and smartphones and consists of six weekly structured sessions. Each session includes brief educational videos and texts, interactive exercises, and a daily sleep diary. Core components are based on the three-factor model of insomnia and CBT-I principles, and include sleep hygiene, stimulus control, sleep restriction, worry management, cognitive restructuring of unhelpful beliefs about sleep, and relapse prevention. Optional adjunct modules provide relaxation and mindfulness audio exercises and additional psychoeducational articles to support self-management and adherence.

Study groups in NCT07431034
Study groupRoleWhat they receive
Omid ICBT-IExperimentalParticipants in this arm will receive access to the Omid Persian-language internet-based cognitive behavioral therapy for insomnia (ICBT-I) program, consisting of weekly web-based modules with psychoeducation about sleep, sleep hygiene, stimulus control, sleep restriction, and cognitive techniques.
Receives: Behavioral: Omid Internet-Based CBT-I Program
Wait-list ControlNo interventionParticipants in this arm will remain on a wait-list and receive usual care during the study period. They will be offered access to the Omid ICBT-I program after completion of the final follow-up assessments.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Insomnia Severity (Insomnia Severity Index, ISI)

    Change in insomnia severity as measured by the Insomnia Severity Index (ISI), a 7-item self-report questionnaire assessing difficulty falling asleep, staying asleep, early morning awakenings, satisfaction with current sleep pattern, interference with daily functioning, perceived noticeability of sleep problem, and level of distress/worry about sleep. Each item is scored 0-4, total scores range 0-28, higher scores indicate greater insomnia severity. Score interpretation: 0-7 = no clinically significant insomnia, 8-14 = subthreshold insomnia, 15-21 = moderate clinical insomnia, 22-28 = severe clinical insomnia.

    Measured: Baseline, Week 6 (immediately post-intervention), and Week 10 (1-month post-intervention follow-up).

  2. Sleep Quality (Pittsburgh Sleep Quality Index, PSQI)

    Change in sleep quality as measured by the Pittsburgh Sleep Quality Index (PSQI), an 18-item self-report questionnaire assessing 7 components of sleep: subjective sleep quality, sleep latency, sleep duration, sleep efficiency, sleep disturbances, use of sleep medications, and daytime dysfunction. Each component is scored 0-3, total scores range 0-21, higher scores indicate poorer sleep quality. A total score >5 indicates poor sleep quality.

    Measured: Baseline, Week 6 (immediately post-intervention), and Week 10 (1-month post-intervention follow-up).

  3. Dysfunctional Beliefs and Attitudes about Sleep (DBAS-10)

    Change in dysfunctional beliefs and attitudes about sleep as measured by the DBAS-10, a 10-item self-report questionnaire assessing maladaptive cognitions and attitudes regarding sleep. Each item is rated on a 5-point Likert scale from 1 ("strongly disagree") to 5 ("strongly agree"). Total scores range 10-50, higher scores indicate more dysfunctional beliefs and attitudes about sleep, which are associated with greater insomnia severity.

    Measured: Baseline, Week 6 (immediately post-intervention), and Week 10 (1-month post-intervention follow-up).

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Feb 2026
  2. Study start21 Feb 2026
  3. Primary completion4 Apr 2026
  4. Study completion4 May 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Two-arm parallel-group randomized controlled trial with a web-based CBT-I intervention (Omid) versus wait-list control.
Masking
None (open label)
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07431034
Sponsor's protocol ID
ICBTI-GEN
Acronym
ICBT-I
Status last verified
Aug 2026
First submitted
16 Feb 2026
Last updated
19 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Omid Internet-Based CBT-I Program in people with Insomnia Disorder and Chronic Insomnia, run by Rasool Hamidi Choolabi at 1 site in Iran.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 19 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Iran. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Insomnia Severity (Insomnia Severity Index, ISI) (time frame: Baseline, Week 6 (immediately post-intervention), and Week 10 (1-month post-intervention follow-up).). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Aug 2026.

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