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N/A N=44 Randomized Basic Science

Oxytocin and Approach-avoid in Grief

Prolonged Grief Disorder · Bereavement

Enrolled (actual)
44
Serious AEs
0.0%
Results posted
Mar 2025
Primary outcome: Primary: Reaction Time (ms) of a Push or Pull of a Joystick in a Standard Interactive Approach/Avoid Task. — 29; 18; 7.5; 13.0 Milliseconds (contrast score)

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Syntocinon (Drug); Placebo (Drug)
Age
Adult, Older Adult · 55+ yrs
Sex
All
Sponsor
University of Arizona
Primary completion
May 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Reaction Time (ms) of a Push or Pull of a Joystick in a Standard Interactive Approach/Avoid Task.
29; 18; 7.5; 13.0

Summary

This is a completed project which was initiated prior to January 18,2017 Background: Theoretical models of complicated grief (CG) suggest that maladaptive approach (e.g., perseverative proximity-seeking of the deceased) or avoidance (e.g., excessive avoidance of reminders) behaviors interfere with a person's ability to integrate the loss and recover from their loved one's death. Due in part to conflicting evidence, little mechanistic understanding of how these behaviors develop in grief exists. We sought to (1) identify behavioral differences between CG and non-CG groups based on implicit bias for grief-, deceased-, and social-related stimuli, and (2) test the role of the neuropeptide oxytocin in shaping approach/avoidance bias. Methods: Widowed older adults with and without CG completed an approach/avoidance task measuring implicit bias for personalized, non-specific, grief-related, and other stimuli. In a double-blinded, randomized, counterbalanced design, each participant attended both an intranasal oxytocin session and a placebo session. Aims were to (1) identify differential effects of CG and stimulus type on implicit approach/avoidance bias [placebo session], and (2) investigate interactive effects of CG, stimulus type, and oxytocin vs. placebo on approach/avoidance bias [both sessions].

Eligibility Criteria

Inclusion Criteria

  • Adult individual experiencing death of a spouse or partner between 6 and 36 months prior to enrollment

Exclusion Criteria

  • Inability to comprehend English;
  • medical contraindications for other components of the study,
  • active suicidality
  • active homicidality
  • active psychotic symptoms
  • ongoing major health conditions such as cancer; uncontrolled hypertension; and medications likely to impact the oxytocin system (e.g., systemic corticosteroids).
  • pregnant status or suspected pregnant status
  • premenopausal status
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04505904). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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