Actively Recruiting

Age: 18Years - 69Years
All Genders
ID06879977

Body Awareness in People With Depressive Disorder

Led by Johannes Kepler University of Linz · Updated on 2025-04-08

125

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying how body awareness is experienced by people with depressive disorders, including depressive episodes and adjustment disorders. This observational study aims to understand the distribution and factors affecting body awareness in this group using the Awareness Body Chart (ABC), a tool designed to assess physical self-awareness. The goal is to gain insights that could support future body-oriented therapies for individuals with depression. Participants are patients with depressive disorders admitted for inpatient care. They will complete various questionnaires, including the ABC, Like/Dislike Body Chart, mood and depression inventories, physical activity, and health surveys, during the first week of admission and again before discharge. The study will analyze changes in body awareness and mood over the course of the inpatient stay. During the study, participants will provide demographic information and complete self-rating questionnaires with or without assistance. Researchers will assess body awareness scores and explore their relationships with demographic, psychological, and physical factors. The study will use statistical tests to compare groups and measure changes in mood and body awareness before and after hospitalization. The total participation is throughout the inpatient stay, with assessments timed at admission and pre-discharge.

CONDITIONS

Brief Title

Body Awareness in People With Depressive Disorder

Who Can Participate

Age: 18Years - 69Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 to 69 years
  • Medical diagnosis of depressive disorder, including depressive episodes and bipolar depression (specific ICD-10 codes)
  • Inpatient admission
  • Ability to provide written informed consent
Not Eligible

You will not qualify if you...

  • Inability to complete questionnaires due to language, physical, or cognitive issues
  • Acute psychotic state
  • Known body schema disorders or significant physical limitations like missing body parts
  • Deafness or blindness

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - Within the first 7 days after admission

Participants complete questionnaires within the first 7 days after admission to assess body awareness, mood, and related factors.

1 visit (inpatient)

Long-term Monitoring

Duration - Duration of inpatient stay

Participants complete follow-up questionnaires before discharge to evaluate changes in body awareness and mood during their inpatient stay.

1 visit (inpatient)

Trial Site Locations

Total: 1 location

1

Kepler University Clinic, Dept. of Physical Medicine & Rehabilitation

Linz, Austria, 4020

Actively Recruiting

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Research Team

C

Christian Mittermaier, M.D.

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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