Istituto Auxologico Italiano IRCCS, Site Piancavallo
Oggebbio, Verbania, 28824, Italy
NCT Number: NCT06800924
The primary objective of the study is to compare the results of the postural and mobility analysis obtained with the use of the Idiag M360 instrument in adult women with anorexia nervosa and in a control group represented by age-matched normal-weight women.
Secondary objectives will be to correlate the results obtained from previous postural analyses with anthropometric parameters, the duration and onset of the disease, and the presence/date of onset of secondary amenorrhea.
This study is active but is not currently recruiting participants.
Notify Me18 year and older
Female
Observational
Oggebbio, Verbania, 28824, Italy
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Anorexia Nervosa:
Inclusion criteria
Exclusion criteria
Normal Weight:
Inclusion criteria
Exclusion criteria
Postural and mobility parameters were obtained with the use of the Idiag M360 scan tool (Idiag, Fehraltorf, Switzerland)
Time frame: Baseline
Idiag M360 scan tool (Idiag, Fehraltorf, Switzerland); flexion expressed in degrees
Time frame: Baseline
IIdiag M360 scan tool (Idiag, Fehraltorf, Switzerland); flexion expressed in degrees
Time frame: Baseline
IIdiag M360 scan tool (Idiag, Fehraltorf, Switzerland); extension expressed in degrees
Time frame: Baseline
IIdiag M360 scan tool (Idiag, Fehraltorf, Switzerland); extension expressed in degrees
This study is active but is not currently recruiting participants.
Notify MeIstituto Auxologico Italiano
Other
Analysis of Posture and Spinal Mobility in Women Suffering From Anorexia Nervosa
Acronym: SPINALAN
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06203418
Anorexia Nervosa, Feeding and Eating Disorders
Chicago, Illinois, United States
View Trial DetailsNCT07757646
Anorexia Nervosa, Autism
London, United Kingdom
View Trial DetailsNCT06259500
Anorexia Nervosa, Feeding and Eating Disorders
Stockholm, Sweden
View Trial DetailsNCT04583774
Anorexia Nervosa, Feeding and Eating Disorders
San Diego, California, United States
View Trial Details