Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
PHASE3
175 participants
INTERVENTIONAL
2012-01-31
2014-04-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Internet-based Cognitive Behavior Therapy for Insomnia for Parents Who Have Lost a Child
NCT02886052
Combined Treatment of Nightmares With Targeted Memory Reactivation and Imagery Rehearsal Therapy
NCT05237778
Internet-CBT for Insomnia
NCT01256099
Nightmare Rescripting and Rehearsal
NCT04529070
Cognitive-Behavioral Therapy for Children With Nightmares
NCT06033781
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Various forms of Cognitive Behavior Therapy (CBT) has been previously shown to be effective against nightmares and among them Imagery Rehearsal Therapy (IRT) has been the most promising. IRT consists of approaching the unpleasant dreams and to imagine a positive ending to them. So far IRT has been compared to untreated controls or treatments that have included methods to some extent similar to those in IRT, and it is therefore difficult to determine the specific effect of IRT.
Since access to CBT therapists is low, different types of self-help treatments for nightmares have been tested, but often these therapies have been provided without the assistance of a therapist, a procedure known to usually lower the effect of self-help treatments. So far, no nightmare treatment has been conducted over the Internet.
IRT will in this study be given as Internet CBT (ICBT) and will be compared to an active and credible control treatment (CONT) consisting of relaxation and exercise to focus on positive images or dreams, but without approaching or reinterpreting the nightmares. Relaxation Training has previously shown preliminary positive effects on nightmares. Both active treatments will be compared to a waiting list which only records how they manage their nightmares (REG).
The main purpose of this study is to examine whether the positive effects of IRT that has been seen in previous studies persists even when IRT is compared with a credible, active control treatment that does not contain the presumed active parts of the IRT. In addition, an untreated control group is used to ensure that the effects are not only due to spontaneous improvement. The control group will afterwards be treated with IRT without therapist support, in order to make a preliminary evaluation of the importance of therapist support.
Some researchers argue that nightmares are not to be seen only as something that is often caused or is a side effect of other conditions, but as a separate problem that should receive special treatment. Our study will help to determine whether it is possible to treat nightmares also in people with other problems such as posttraumatic stress disorder (PTSD).
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
IRT
Imagery Rehearsal Therapy
IRT
Internet-based IRT with therapist support during 6 weeks
CONT
Stress reduction and positive imagery
Stress Reduction
Internet-based stress reduction with therapist support during 6 weeks
REG
Registration only
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
IRT
Internet-based IRT with therapist support during 6 weeks
Stress Reduction
Internet-based stress reduction with therapist support during 6 weeks
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* experience significant discomfort or distress due to nightmares/unpleasant dream.
* the content of the nightmares are not only related to a previous trauma.
* at least 18 years
* speaks, writes and read Swedish
* can not foresee any practical barriers to participation.
Exclusion Criteria
* has a high alcohol or drug use assessed by the AUDIT / DUDIT and assessment interview.
* somatic or psychiatric problems that are directly contraindicated or seriously hamper the implementation of the treatment (eg, psychotic disorders).
* have severe depression, defined as MADRS-S over 30 or suicidal risk judged by more than 4 points on the MADRS-S question 9 or according to the structured telephone assessment.
* has a total score over 76 on the IES-R (one standard deviation above the mean for individuals with a diagnosis of PTSD).
* is diagnosed with PTSD and can not provide proof that they have a current health care contact regarding PTSD.
* suffer from intrusive images or flashbacks during their waking hours (regardless of a PTSD diagnosis).
* currently undergoing some form of treatment that focuses on reducing symptoms of nightmares.
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Region Stockholm
OTHER_GOV
Karolinska Institutet
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Viktor Kaldo
Principal Investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Viktor Kaldo, Ph.D
Role: PRINCIPAL_INVESTIGATOR
Karolinska Institutet
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Internetpsykiatrienehten (Internet Psychiatry Unit), Psykiatri Sydväst, SLSO
Stockholm, , Sweden
Countries
Review the countries where the study has at least one active or historical site.
Related Links
Access external resources that provide additional context or updates about the study.
The public page of the Internet-CBT treatment platform
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
ICBT_Nightmares
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.