Anorexia Nervosa and Brain in Adolescence

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age16-19
SponsorKuopio University Hospital

About this trial

Aims of this follow-up study are to investigate effects of anorexia nervosa on brain structure and functions in adolescence.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

Target study population is 50 participants. Study group (25 participants) are recruited from North Savo wellbeing services, Adolescent psychiatry outpatient clinic. Control group (25 participants) are recruited from Kuopio restrict lower and upper secondary schools.

Trial design

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

  • Observational study methods

    Other intervention

    Neuroimaging, body compostion, laboratory tests and psychiatric interview in study and in control groups.

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: Study group1 intervention
Group B: Control Group1 intervention

Trial outcomes

Primary outcomes

1

Neuroimaging

Transcranial magnetic stimulation (TMS) combined with electroencephalogram (EEG)

Time frame
Baseline and at 3 years' follow-up

Secondary outcomes

1

Neuroimaging

Magnetic resonance imaging (MRI)

Time frame
Baseline and at 3 years' follow-up

Other outcomes

1

Psychiatric evaluation

Self-rated questionnaires measuring somatic and mentalh health (such as EDE-Q, BDI, substance use measurements) and structured psychiatric diagnostic interview (SCID)

Time frame
Baseline and at 3 years' follow-up
2

Body composition measurement

InBody body composition measurement (non-invasive method to measure information about the quantity and segmentation of muscle, bone and fat tissue in body and about your basal metabolic rate)

Time frame
Baseline and at 3 years' follow-up
3

Laboratory tests

Blood sample (markers describing undernourishment, more precise description before study)

Time frame
Baseline and at 3 years' follow-up

Locations

This trial has no locations.

Sponsors and contacts

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