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Pilot Internet-based Self-Help Program for Managing Corona (COVID-19) Stress

Pilot Internet-based Self-Help Program for Managing Corona Stress vs. Waitlist Control

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04394403
Acronym
CoronaStress
Enrollment
120
Registered
2020-05-19
Start date
2020-05-14
Completion date
2022-06-30
Last updated
2021-02-09

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

Conditions

Stress, Stress, Psychological

Brief summary

The current study examines an adapted guided self-help stress reduction program, focusing on reducing stress in the time of COVID-19. Two studies are planned: 1) an international study in English in which individuals proficient in English throughout the world will participate and 2) a follow-up study in Hebrew.

Detailed description

The current study examines an adapted guided self-help stress reduction program, focusing on reducing stress in the time of COVID-19. Two studies are proposed: 1) an international study in English in which individuals proficient in English throughout the world will participate and 2) a study in Hebrew. The first study will publicize via social media and participants will be randomized to either immediate participation or a 6 week waitlist period. Assessments will be conducted pre, (again after waitlist for the control group), posttx (after completion/cessation of the program), 6 month and 1 year followup. Two forms of assessment will be conducted: pre-post-follow-up (with the CRISIS measure) and weekly during the program (via the DASS-21). For the full program see: https://www.iterapi.se/sites/coronastress/

Interventions

BEHAVIORALInternet-based guided self-help based on CBT principles

Individuals are provided basic rationale of CBT to deal with stress, worry, anxiety, dysphoria, sleep difficulties, emotion dysregulation, and memories all related to COVID-19

Sponsors

Hebrew University of Jerusalem
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

This is a randomized trial to either immediate or delayed access to the internet guided self-help program

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Read/Write English, * feels stress due to Corona/COVID-19

Exclusion criteria

* current psychological or psychiatric treatment, * current psychiatric illness, * suicidality, * psychosis, * bipolar, * severe dissociative symptoms, * in a currently severe traumatic situation, * having a serious medical illness.

Design outcomes

Primary

MeasureTime frameDescription
The CoRonavIruS Health Impact Survey (CRISIS)change from Pre to post treatment (6 weeks),change in a self-report measure of stress during the COVID-19 pandemic that ranges from 0-128. Higher means more symptomatic.

Secondary

MeasureTime frameDescription
Depression, Anxiety, and Stress Scale- 21 item version: DASS-21Weekly change during treatment and at pre and post (6 week) treatment evaluationsa self-report measure of depression, anxiety and stress, with each subscale ranging from 0-28. Higher means more symptomatic.

Other

MeasureTime frameDescription
completion rate of modules6 weekshow many modules each individual completes, with less than 2 being considered dropout

Countries

Israel

Contacts

Primary ContactJonathan Huppert, PhD
jonathan.huppert@mail.huji.ac.il+97225883376

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026