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临床试验/NCT03900754
NCT03900754
终止
2 期

A Pharmaco-imaging Approach to Predicting Social Functioning and Clinical Responses to Oxytocin Administration in Schizophrenia

VA Office of Research and Development2 个研究点 分布在 1 个国家目标入组 26 人2020年1月13日
适应症Schizophrenia
干预措施OxytocinPlacebo
相关药物OxytocinPlacebo

概览

阶段
2 期
干预措施
Oxytocin
疾病 / 适应症
Schizophrenia
发起方
VA Office of Research and Development
入组人数
26
试验地点
2
主要终点
Social Functioning Score
状态
终止
最后更新
3个月前

概览

简要总结

Schizophrenia has a devastating and disproportionate effect on veterans compared to the general US population. Some of the most disabling symptoms, such as low motivation, difficulty expressing emotions, and decreased ability to infer the mental states of others, cause poor social functioning. This means that veterans with schizophrenia have trouble navigating interpersonal interactions and building meaningful relationships in the community. Unfortunately, current antipsychotic medications typically only improve positive symptoms but fail to improve social functioning deficits, which are strong predictors of poor quality of life and functional outcomes. Oxytocin, a peptide found in the brain, plays an important role in social behavior and is known to moderate affiliation, stress, and learning across taxa. In this study, the investigators will test whether oxytocin could be an effective treatment for social functioning deficits in schizophrenia. The investigators will examine changes in brain activation to understand how oxytocin affects behavior and to predict which individuals may benefit from oxytocin treatment.

详细描述

The study uses a combined within- and between-subject placebo-controlled study design. Within subjects phase: After screening, participants will be randomized into two study arms for the fMRI phase of the study. In each study arm, participants will complete a placebo-controlled, within-subject, pharmaco-fMRI paradigm with one of two possible dosages of oxytocin (20 or 40IU) and placebo. Following the fMRI phase of the study, participants will be randomized for the next phase of the study Between subjects phase: Participants will receive the same dosage of oxytocin the participant received in the fMRI phase, or placebo, twice daily for 3 weeks. Before and after the three weeks of drug administration, participants will be assessed for social functioning, social ability, negative symptoms, and theory of mind. More participants will be randomized to receive chronically administered oxytocin than placebo to maximize the study's power to test the investigators' hypothesis that acute oxytocin-induced increases in right temporo-parietal junction activity will be positively correlated with improvements in social functioning (primary outcome), social ability, negative symptoms, and theory of mind over three weeks of oxytocin administration.

注册库
clinicaltrials.gov
开始日期
2020年1月13日
结束日期
2024年1月31日
最后更新
3个月前
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

责任方
Sponsor

入排标准

入选标准

  • age 18-70
  • a diagnosis of schizophrenia, schizophreniform, schizoaffective, or brief psychotic disorder determined by the Structured Clinical Interview for DSM-5
  • no medication changes or psychiatric hospitalizations in the past month
  • SFS modified raw score of no more than 75

排除标准

  • substance use disorder in the past month, except mild to moderate cannabis use disorder
  • illness affecting the nasal passages
  • significant neurological/medical disorder
  • pacemakers
  • extensive dental work
  • claustrophobia
  • inability to read
  • currently participating in a psychosocial intervention targeting social functioning deficits
  • currently taking high dose testosterone or estrogen/progesterone
  • inability to complete VOT

研究组 & 干预措施

Intranasal Oxytocin

Dosages of oxytocin: 20IU or 40IU.

干预措施: Oxytocin

Placebo

Saline

干预措施: Placebo

结局指标

主要结局

Social Functioning Score

时间窗: From the baseline visit in the chronic OT administration portion of the study design to after three weeks of oxytocin administration

The Social Functioning Scale is a 79-item semi-structured interview based assessment that includes \[a global summary score (primary outcome) as well as seven subscales (secondary outcomes): social engagement, interpersonal communication, independence, competence, recreation, prosocial, and employment.\] A mean of the subscale scores provides overall score of social functioning. Each subscale score is transformed into a standard distribution with a mean of 100 and standard deviation of 15 for comparability and interpretation. Higher scores indicates a high level of functioning.

次要结局

  • CAINS Score (clinical assessment interview for negative symptoms)(From the baseline visit in the chronic OT administration portion of the study design to after three weeks of oxytocin administration)

研究点 (2)

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