Skip to content

The Remote Family Support Programs for Eating Disorders

The Effectiveness of a Remote Family Support Programs for Families of Patients With Eating Disorders

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05840614
Enrollment
67
Registered
2023-05-03
Start date
2023-03-18
Completion date
2024-10-30
Last updated
2025-07-29

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

Conditions

Eating Disorders

Keywords

Family support, Interpersonal psychotherapy

Brief summary

Eating disorders are serious mental health disorders associated with high levels of mortality, disability, physical and psychological morbidity, and impaired quality of life. Family members who spend the majority of their time with patients of eating disorders experience heavy psychological burden. Remote family support programs consist of interpersonal psychotherapy and family psychoeducation. This study aimed to examine the effectiveness of a remote family support program for eating disorders in an RCT (randomized controlled trial). The specific objective was to conduct a small pilot RCT of the remote family support program (n=28) compared with TAU (n=28).

Interventions

BEHAVIORALThe remote family support program

Remote family support programs consist of interpersonal psychotherapy (IPT) and family psychoeducation. Each session consisted of a lecture, followed by role playing and supportive group therapy. In the first session, we informed the participants about the symptoms of eating disorders and mechanism of IPT; in the second session, we shared details about the characteristics of adolescents; and during the third and fourth sessions, we provided information on effective communication according to IPT.

Sponsors

Nagoya City University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* The research participants are parents of patients who have been diagnosed with an eating disorder by a physician or have symptoms of an eating disorder; parents may or may not be related by blood. * The ABOS score measured by the research participants at enrollment is over 8 points. * Patient age at enrollment ranged from 12 to 29 years. * The patient has lived with their parents at the time of participating in this study and is expected to live with them during the investigation period. * Patients may or may not undergo treatment. * Patients with other psychiatric comorbidities are included. * Participants with other psychiatric comorbidities are included. * If multiple family members (e.g., parents) participated in this program, the primary participant is determined, and that person becomes the target research participant. * Willingness to provide informed consent and comply with the trial protocol.

Exclusion criteria

* The participants cannot read or write in Japanese * The participants cannot use the Zoom meeting system * Researcher of this study and their families

Design outcomes

Primary

MeasureTime frameDescription
Change in the total Active Listening Attitude Scale (ALAS) score of participantsBase-line, four weeks, and eight weeksThe ALAS comprises 2 subscales and 20 items: listening attitude (10 items) and listening skills (10 items). Higher the scores indicate better listening attitudes or skills.

Secondary

MeasureTime frameDescription
Change in the total Social Provisions Scale-10 item (SPS-10) score of participantsBase-line, four weeks, and eight weeksParents' perception of social support is measured using SPS-10.

Other

MeasureTime frameDescription
LonelinessBase-line, four weeks, and eight weeksParents' loneliness is evaluated using the University of California Los Angeles Loneliness Scale (ULS).
Mental healthBase-line, four weeks, and eight weeksPsychological distress experienced by the participants is assessed using the Kessler Psychological Distress Scale (K6).
Family functioningBase-line, four weeks, and eight weeksFamily functioning is assessed using the Family Assessment Device (FAD).
Eating disorder behaviorsBase-line, four weeks, and eight weeksInformation on behaviors and attitudes of patients with eating disorders obtained from their parents is measured using the Anorectic Behavior Observation Scale (ABOS).

Countries

Japan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026