Birchwood Social Function Scale (BSFS) Total Score
| Group | Value (units on a scale) | Spread |
|---|---|---|
| CBSST + Oxytocin | 120 | 23.1 |
| CBSST + Placebo | 115.8 | 21.4 |
Trial · Interventional
CompletedNot applicableResults postedRegistry dataUnited States
1 trial · 1 completed · 1 with posted results
Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.
A significant proportion of people with schizophrenia are characterized by impaired ability to socially engage with others, which may reflect social aversion secondary to defeatist beliefs; decreased motivation for social interactions; and/or impairment in the normal reinforcement value of social interactions. These impairments in social function have been shown to be associated with social skill deficits; and decreased ability to identify and remember emotional facial expressions and empathize with the emotional status of others. Unfortunately, pharmacological interventions have limited benefits for impaired social function, whereas psychosocial interventions provide only partial benefit for this critical aspect of the illness. The development of an effective intervention for functional outcomes remains a central therapeutic challenge. Cognitive Behavioral Social Skills Training (CBSST) uses corrective feedback and reinforcement provided by successful interactions to challenge and reduce defeatist performance beliefs that contribute to low drive and interfere with social functioning. CBSST has been shown to have modest effects on social function in people with schizophrenia. Oxytocin plays a critical role in the regulation of normal social affiliative behavior; it is hypothesized to enhance social affiliation through the reduction of anxiety or social risk aversion; the enhancement of motivation for prosocial approach behavior; and/or increased modulation of the salience and processing of social cues. People with schizophrenia have decreased oxytocin levels, which are associated with an impaired ability to identify facial emotions and decreased prosocial behaviors. The study will be comprised of three phases: 1) 2-week Evaluation Phase; 2) 24-week Double-blind Treatment Phase; and 3) 3-month Follow-up Phase.
Experimental
CBSST + oxytocin
Cognitive Behavioral Social Skills Training with adjunct oxytocin nasal spray treatment. Participants will receive 80 IU/day of oxytocin administered intranasally in two doses (40 IU morning and evening).
Placebo comparator
CBSST + placebo
Cognitive Behavioral Social Skills Training with placebo nasal spray. The placebo nasal spray bottles will be matched in appearance to the oxytocin nasal spray bottles and similarly administered intranasally in two doses (morning and evening).
Outcomes the sponsor listed as primary.
Birchwood Social Function Scale (BSFS) Total Score
Time frame · Treatment weeks 0, 12, and 24, plus follow-up week 36
Determine if CBSST + oxytocin compared to CBSST + placebo is associated with improved social function. There are 7 individual sections, with each section asking about different aspects of social functioning. Scores for Section 1: "Social Engagement Withdrawal" range from 0-15; Section 2: "Interpersonal Communication/Relationships" ranges from 0-30; Section 3: "Prosocial Activities" range is 0-66; Section 4: "Recreation" ranges from 0-48; Section 5: "Independence (Performance)" ranges from 0-39; Section 6: "Independence (Competence)" ranges from 0-39; and Section 7: "Occupation/Employment" ranges from 0-6 if the participant is unemployed or 7-10 if the participant is employed. The minimum value possible is 0 for participants who are unemployed and 7 for those with employment. The total BSFS score is calculated by adding the total scores from each of the 7 sections, with a maximum total score of 247. A lower total score indicates a lower social function rating.
Defeatist Performance Attitudes Scale (DPAS) Total Score
Time frame · Treatment weeks 0, 12, and 24, plus follow-up week 36
Determine if CBSST + oxytocin compared to CBSST + placebo is associated with defeatist performance beliefs. The total DPAS score is calculated by adding the scores for scales #1-#18. Each scale ranges from "1=Agree Totally" to "7=Disagree Totally". Total scores range from a minimum score of 18 to a maximum score of 126. Reverse scoring was applied to make higher scores indicate a stronger defeatist attitude.
Asocial Belief Scale (ABS) Total Score
Time frame · Treatment weeks 0, 12, and 24, plus follow-up week 36
Determine if CBSST + oxytocin compared to CBSST + placebo is associated with asocial beliefs. The total ABS score is calculated by adding the scores for items #1-#15. Each scale is provided a True/False response, with True responses equaling 1 point and False responses equaling 0 points. In calculating the ABS total score, four of the 15 items of the ABS were reverse scored. A lower total score indicates more severe asocial beliefs.
Schedule for Assessment of Negative Symptoms (SANS) Total Score
Time frame · Every 4 weeks during the treatment phase, plus follow-up week 36
SANS total score range = 0-85. Higher scores indicate more severe negative symptoms.
Brief Psychiatric Rating Scale (BPRS) Total Score
Time frame · Every 4 weeks during the treatment phase, plus follow-up week 36
The total BPRS score is calculated by adding the scores for scales #1-#18. Each scale ranges from "1=Not Present" to "7=Very Severe". Total scores range from a minimum score of 18 to a maximum score of 126. A higher total score indicates a more severe psychiatric symptom rating.
Brief Psychiatric Rating Scale (BPRS) Psychosis Score
Time frame · Every 4 weeks during the treatment phase, plus follow-up week 36
The psychosis score is calculated by adding the scores for scales #4 Conceptual Disorganization, #11 Suspiciousness, #12 Hallucinatory Behavior, and #15 Unusual Thought Content. Each scale ranges from "1=Not Present" to "7=Very Severe". The minimum psychosis score is 4 and the maximum psychosis score is 28. A higher score indicates a more severe psychosis rating.
Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.
| Group | Value (units on a scale) | Spread |
|---|---|---|
| CBSST + Oxytocin | 120 | 23.1 |
| CBSST + Placebo | 115.8 | 21.4 |
| Group | Value (units on a scale) | Spread |
|---|---|---|
| CBSST + Oxytocin | 68.55 | 19.23 |
| CBSST + Placebo | 67.87 | 15.31 |
| Group | Value (units on a scale) | Spread |
|---|---|---|
| CBSST + Oxytocin | 6.8 | 3.6 |
| CBSST + Placebo | 5.5 | 2.5 |
| Group | Value (units on a scale) | Spread |
|---|---|---|
| CBSST + Oxytocin | 28.5 | 12.5 |
| CBSST + Placebo | 35.9 | 12.5 |
| Group | Value (units on a scale) | Spread |
|---|---|---|
| CBSST + Oxytocin | 38.2 | 8.2 |
| CBSST + Placebo | 40.0 | 10.4 |
| Group | Value (units on a scale) | Spread |
|---|---|---|
| CBSST + Oxytocin | 10.4 | 4.9 |
| CBSST + Placebo | 11.7 | 6.0 |
| Group | Deaths | Serious events | Other events |
|---|---|---|---|
| CBSST + OxytocinCognitive Behavioral Social Skills Training with adjunct oxytocin nasal spray treatment. Participants will receive 80 IU/day of oxytocin administered intranasally in two doses (40 IU morning and evening). CBSST + Oxytocin: The oxytocin dose of 80 IU/day, will be administered in two divided doses: 40 IU in the morning and 40 IU in the evening. Oxytocin will be administered intranasally (10 puffs of the spray, 5 in each nostril at each administration). CBSST groups will occur for an hour twice/week. Nasal spray will be administered an hour prior to the CBSST group. | – | 1 / 31 | 3 / 31 |
| CBSST + PlaceboCognitive Behavioral Social Skills Training with placebo nasal spray. The placebo nasal spray bottles will be matched in appearance to the oxytocin nasal spray bottles and similarly administered intranasally in two doses (morning and evening). CBSST + Placebo: Matching placebo spray will be administered intranasally (10 puffs of the spray, 5 in each nostril at each administration). CBSST groups will occur for an hour twice/week. Nasal spray will be administered an hour prior to the CBSST group. | – | 0 / 31 | 5 / 31 |
Each cell reads participants affected / participants at risk, as the registry posted them.
Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works
Studies that cite this trial.
1 study on this page
Indexing hint: Randomized controlled trial · 2021
Buchanan et al. 2021Journal of clinical psychopharmacologycited by 19
PMID 33783399PMC8887701DOI 10.1097/jcp.0000000000001397PUB-33783399
Who could join, as posted.
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