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A pilot randomized controlled trial of omega-3 fatty acid supplementation for the treatment of anxiety in adolescents with anorexia nervosa.


ABSTRACT: OBJECTIVE:To evaluate the effectiveness and tolerability of omega-3 polyunsaturated fatty acid (PUFA) supplementation for treatment of trait anxiety among adolescent females with restrictive anorexia nervosa (AN). METHOD:A pilot double-blind, placebo-controlled randomized trial of adolescent females with AN (N?=?24) entering Partial Hospitalization Program (PHP) from January 2015 to February 2016. Participants were randomized to four daily PUFA (2,120?mg eicosapentaenoic acid/600?mg docosohexaenoic acid) or placebo capsules for 12?weeks. A 9-item questionnaire of side effect frequency assessed medication tolerability. The Beck Anxiety Inventory-Trait measured anxiety at baseline, 6, and 12?weeks. Linear mixed models evaluated associations between randomization group and study outcomes. Twenty-two and 18 participants completed 6 and 12?weeks of data collection, respectively. RESULTS:Medication side effect scores were low and were not significantly different between randomization groups at Week 6 (p?=?.20) or 12 (p?=?.41). Mean trait anxiety score significantly (p?

SUBMITTER: Manos BE 

PROVIDER: S-EPMC7061649 | biostudies-literature | 2018 Dec

REPOSITORIES: biostudies-literature

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A pilot randomized controlled trial of omega-3 fatty acid supplementation for the treatment of anxiety in adolescents with anorexia nervosa.

Manos Brittny E BE   Bravender Terrill D TD   Harrison Tondi M TM   Lange Hannah L H HLH   Cottrill Casey B CB   Abdel-Rasoul Mahmoud M   Bonny Andrea E AE  

The International journal of eating disorders 20181026 12


<h4>Objective</h4>To evaluate the effectiveness and tolerability of omega-3 polyunsaturated fatty acid (PUFA) supplementation for treatment of trait anxiety among adolescent females with restrictive anorexia nervosa (AN).<h4>Method</h4>A pilot double-blind, placebo-controlled randomized trial of adolescent females with AN (N = 24) entering Partial Hospitalization Program (PHP) from January 2015 to February 2016. Participants were randomized to four daily PUFA (2,120 mg eicosapentaenoic acid/600   ...[more]

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