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Evaluation of an online cognitive-behavioral therapy for insomnia and anxiety in older adults

Online cognitive-behavioral therapy (CBT) for insomnia and anxiety in older adults: a pilot study using e-SPACE, a multidomain web platform for health promotion

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN15338211
Enrollment
60
Registered
2021-12-13
Start date
2021-07-01
Completion date
Unknown
Last updated
2026-05-19

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

Conditions

Older adults with insomnia or anxiety symptoms. Mental and Behavioural Disorders

Interventions

Participants will be divided using a stratified (sex and use of medication) randomization method using an online tool. Updated 24/01/2022: Participants will be divided using a stratified (Geriatric A

Sponsors

Institut Universitaire de Gériatrie de Montréal
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Current inclusion criteria as of 24/01/2022: 1. Aged =65 years 2. Insomnia Severity Index score >7 3. Ability to read and understand French 4. Reliable internet access 5. Ability to use a smartphone, tablet, or computer Previous inclusion criteria: 1. Aged =65 years 2. Mild symptoms of insomnia (Insomnia Severity Index score >8) or anxiety (Generalized Anxiety Disorder 7 score >5) 3. Ability to read and understand French 4. Reliable internet access 5. Ability to use a smartphone, tablet, or computer

Exclusion criteria

Exclusion criteria: 1. Currently hospitalized or expected to require hospital admission within 3 months 2. Suicidal thoughts 3. Uncorrected and severe hearing or vision impairment 4. Diagnosis of major neurocognitive disorder or bipolar disorder

Design outcomes

Primary

MeasureTime frame
Current primary outcome measures: 1. User satisfaction, defined as the level of comfort felt by the user when using the program and what the user thinks about different functionalities, measured using an adapted version of the System Usability Scale (SUS) at 8 weeks 2. User acceptance, defined as the extent to which the user is eager to adopt the web-based solution in the future, measured using an adapted version of the Technology Acceptance Model-2 (TAM-2) questionnaire at 8 weeks Previous primary outcome measures: 1. User efficiency, defined as the time for task completion and frequency of clicks on the wrong button, collected through the platform during the 8-week intervention 2. User satisfaction, defined as the level of comfort felt by the user when using the program and what the user thinks about different functionalities, measured using an adapted version of the System Usability Scale (SUS) at 8 weeks 3. User acceptance, defined as the extent to which the user is eager to adopt the web-based solution in the future, measured using an adapted version of the Technology Acceptance Model-2 (TAM-2) questionnaire at 8 weeks

Secondary

MeasureTime frame
Current secondary outcome measures as of 24/01/2022: Intervention effectiveness measured using the following: 1. Sleep efficiency measured using sleep diaries at baseline and 8 weeks 2. Insomnia measured using the insomnia severity index (ISI) at baseline and 8 weeks 3. Anxiety measured using the Geriatric Anxiety Inventory (GAI) at baseline and 8 weeks Previous secondary outcome measures: Intervention effectiveness measured using the following: 1. Sleep efficiency measured using sleep diaries at baseline and 8 weeks 2. Insomnia measured using the insomnia severity index (ISI) at baseline and 8 weeks 3. Anxiety measured using the Geriatric Anxiety Inventory (GAI) and Generalised Anxiety Disorder Assessment (GAD-7) at baseline and 8 weeks

Countries

Canada

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: May 22, 2026