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The Acceptability and Effectiveness of Receiving a Low-intensity Self-guided Psychoeducational Intervention for Individuals Waitlisted for Specialized Eating-disorder Treatment

The Acceptability and Effectiveness of a Virtual Psychoeducational Intervention for Individuals Waitlisted for Specialized Eating Disorder Treatment

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07319936
Enrollment
78
Registered
2026-01-06
Start date
2023-05-09
Completion date
2025-04-03
Last updated
2026-01-06

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

Conditions

Eating Disorders

Keywords

psycho-education, eating disorders, self-help

Brief summary

It is often difficult for people with eating disorders to get timely access to specialized treatment, as waitlists can be long. The present study examines whether or not providing educational materials by email could help individuals with eating disorders while they wait for specialized care. The investigators hypothesize that a low-intensity self-guided intervention will lead to a reduction in eating-disorder attitudes and cognitions, and an increase in motivation to change and body satisfaction. Sixty-two adults (primarily women) are randomly assigned to one of two groups while being on the waitlist for specialized eating-disorder services. One group receives weekly emails for four weeks with psychoeducational materials about eating disorders; the other group does not receive any materials. The content was adapted from a validated eating-disorder workbook developed by the Centre for Clinical Interventions in Australia and translated into French. Each week, as well as one week after the intervention period, all participants complete brief questionnaires assessing eating-disorder thoughts, body satisfaction, and readiness to make changes in eating behaviours. Participants who receive the materials also rate their level of satisfaction with the materials as well as how useful and engaging they find the content.

Interventions

Receives weekly psychoeducation related to eating disorders via email, while on the waitlist for treatment \[experimental condition\].

BEHAVIORALNo psycho-education

Does not receive any psychoeducational materials, while on the waitlist for treatment \[control condition\].

Sponsors

Douglas Mental Health University Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1\. Between 18-65 years and have a diagnosis of Anorexia Nervosa, Bulimia Nervosa or Other Specified Feeding or Eating Disorders (OSFED) as defined by DSM-5 criteria.

Exclusion criteria

* Current substance use disorder * Comorbid psychotic disorder * Major physical symptoms that could interfere with the intervention or or requiring urgent care (referred to priority 1 during phone evals) * Body mass index lower than 15 * Pregnancy * Insufficient access to the internet (by phone, tablet or computer) to complete the intervention * Not being able to access 2-3 modules for 4 consecutive weeks. Information on presence of current substance use disorder, comorbid psychotic disorder, major physical symptoms, body mass index and pregnancy are based on information from the clinical referal form and information from the initial screening for treatment eligibility in the eating-disorder program.

Design outcomes

Primary

MeasureTime frameDescription
Eating Disorder-15Weekly, from enrollment to the end of the study at week 5 (week 0, 1, 2, 3, 4, 5)10 items that assess eating-disorder symptoms, each rated on a 7-point Likert frequency scale, ranging from 0 (not at all) to 7 (all the time). A higher score means more symptoms.
Body Satisfaction ScaleWeekly, from enrollment until the last time the materials were offered (week 0, 1, 2, 3, 4).State-related changes in body satisfaction are assessed using the Body Dissatisfaction subscale of the Body Satisfaction Scale (BSS). The subscale asks participants to indicate their level of satisfaction with seven body parts (e.g., chest, tummy, legs, etc.) at the time of questionnaire completion on a 7-point Likert scale (1 = very satisfied to 7 = very unsatisfied). A higher score means more symptoms.
Readiness RulerWeekly, from enrollment until the last time the materials were offered (week 0, 1, 2, 3, 4).The readiness ruler is an 18-item questionnaire, aimed at measuring state-related motivation. The readiness ruler measures readiness to change across nine eating-disorder related attitudes (restriction, weight-shape overevaluation, binge eating, vomiting, laxative use, fasting, diuretic use, weight-gain phobia, and exercise) on a scale from 1 to 10. A higher score means more readiness to make changes.
Eating Disorder Examination QuestionnaireWeekly, from enrollment to the end of the study at week 5Questionnaire measuring global eating-disorder severity. The questionnaire is being used to assess severity. The responses on the EDE-Q are also used to corroborate the provisional eating-disorder diagnosis at baseline. The questionnaire asks about symptoms the past 28 days and a higher score means more symptoms. The scores on each item ranges from 0 to 6. 0 = no days; 1 = 1-5 days; 2 = 6-12 days; 3 = 13-15 days; 4 = 16-22 days; 5 = 23-27 days; 6 = 28 days.

Other

MeasureTime frameDescription
Compliance, satisfaction and engagement with the materialsAfter having received 2 and 4 weeks of psychoeducational materials (week 2 and 4).Items are adjusted from the Homework Rating Scale. Participants in the experimental condition are asked to rate how many modules they did, with 0=none, 1=a few, 2=many, 3=most, and 4=all. The questionnaire also include items assessing level of engagement, enjoyment, perceived control over problems, and anticipated future use. Items are scored as 0=not at all, 1=somewhat, 2=moderately, 3=very, and 4=extremely. A higher scoremeans more engagement, enjoyment, perceived control over problems, and anticipated future use.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 5, 2026