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Can Mindfulness and Self-monitoring Improve Control Over Maladaptive Daydreaming?

U

University of Haifa

Status

Completed

Conditions

Psychological Intervention
Intervention Study
Internet-Based Intervention

Treatments

Other: Online therapeutic intervention for maladaptive daydreaming based on mindfulness
Other: Online therapeutic intervention for maladaptive daydreaming based on mindfulness and self-monitoring

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Maladaptive daydreaming (MD) is a compulsive form of daydreaming that causes distress and functional impairment among tens of thousands of self-diagnosed sufferers. This is the first controlled treatment trial for MD. The investigators built an internet-based self-help program for MD and tested the effectiveness of mindfulness and self-monitoring in improving control over MD, comparing three groups across three measurement points in time.

Full description

Objective: Maladaptive daydreaming (MD) is a compulsive form of daydreaming that causes distress and functional impairment among tens of thousands of self-diagnosed sufferers. This is the first controlled treatment trial for MD. Method: The investigators built an internet-based self-help program for MD and tested the effectiveness of mindfulness and self-monitoring in improving control over MD, compared to internet-based support as usual (waiting-list group). Participants were randomly assigned to three groups and measured across three points in time (baseline, post-intervention, and 6 months follow-up). The investigators measured the change in daydreaming pathology (MDS-16), daydreaming frequency (DDFS), and daydreaming functioning (DWSAS), alongside changes in psychiatric symptoms (BSI), and intervention outcome (OQ). Changes in mindful attention and awareness skills, compliance with program requirements, and feedback to the program were also measured.

Enrollment

697 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age above 18 years
  • MD diagnosis
  • Not being in any concurrent treatment for MD
  • English fluent
  • Daily access to the internet, and to a device with internet access
  • Give informed consent to the study
  • Respondents who reported being on a stable dose of medication for at least three months could take part in the study provided that they did not change their dosages while participating in the study.

Exclusion criteria

  • Age under 18 years
  • No MD diagnosis
  • In concurrent psychology therapy for MD
  • Not fluent in English
  • Not having a daily internet access
  • Taking medication for less than three months

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

697 participants in 3 patient groups

The Full Intervention (FI) group
Experimental group
Description:
The full intervention (FI) group received a psycho-education module about MD and its addictive behavior mechanism, a motivation enhancement module based on motivational interviewing, mindfulness modules, and self-monitoring modules.
Treatment:
Other: Online therapeutic intervention for maladaptive daydreaming based on mindfulness and self-monitoring
The partial intervention (PI) group
Active Comparator group
Description:
The partial intervention (PI) group received an intervention identical to the FI group (a psycho-education module about MD and its addictive behavior mechanism, a motivation enhancement module based on motivational interviewing, mindfulness modules) with the exclusion of the self-monitoring modules.
Treatment:
Other: Online therapeutic intervention for maladaptive daydreaming based on mindfulness
Waiting List (WL) group
No Intervention group
Description:
Waiting List (WL) group did not undergo any intervention during the study period. However, WL participants were told that the program will commence in three months. During their waiting time participants were instructed to reduce their daydreaming activity to the best of their ability. Since all participants were recruited for this study from an online support forum (that is not part of this research design), the investigators labeled WL as the Internet Support as Usual (ISAU) group.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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