Trial · NCT04230577
Registered outcomes92
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
81 to 92 of 92
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Secondary | Quality of Community Integration Questionnaire Cognitive Quality of Life Score 1 | Change from Pre-Treatment Baseline to 1-Week after Series 1 | Cognitive Quality of Life Score: Cognitive Satisfaction Score x score on item 16. Range: 6 - 72 |
| Secondary | Quality of Community Integration Questionnaire Cognitive Quality of Life Score 2 | Change from Pre-Treatment Baseline to 1-Month after Series 1 | Cognitive Quality of Life Score: Cognitive Satisfaction Score x score on item 16. Range: 6 - 72 |
| Secondary | Quality of Community Integration Questionnaire Cognitive Quality of Life Score 3 | Change from 1-Week to 1-Month after Series | Cognitive Quality of Life Score: Cognitive Satisfaction Score x score on item 16. Range: 6 - 72 |
| Secondary | Quality of Community Integration Questionnaire Cognitive Quality of Life Score 4 | Change from Pre-Treatment Baseline to 1-Week after Series 2 | Cognitive Quality of Life Score: Cognitive Satisfaction Score x score on item 16. Range: 6 - 72 |
| Secondary | Dysexecutive Functional Index (DEX) 1 | Change from Pre-Treatment Baseline to 1-Week after Series 1 | Self-Report of psychosocial problems that participant may be experiencing in everyday life. 20 Questions Scale of 0-4 for each item Total Possible: 80 Lower Score = better outcome |
| Secondary | Dysexecutive Functional Index (DEX) 2 | Change from Pre-Treatment Baseline to 1-Month after Series 1 | Self-Report of psychosocial problems that participant may be experiencing in everyday life. 20 Questions Scale of 0-4 for each item Total Possible: 80 Lower Score = better outcome |
| Secondary | Dysexecutive Functional Index (DEX) 3 | Change from 1-Week to 1-Month after Series | Self-Report of psychosocial problems that participant may be experiencing in everyday life. 20 Questions Scale of 0-4 for each item Total Possible: 80 Lower Score = better outcome |
| Secondary | Dysexecutive Functional Index (DEX) 4 | Change from Pre-Treatment Baseline to 1-Week after Series 2 | Self-Report of psychosocial problems that participant may be experiencing in everyday life. 20 Questions Scale of 0-4 for each item Total Possible: 80 Lower Score = better outcome |
| Secondary | Tinnitus Functional Index 1 | Change from Pre-Treatment Baseline to 1-Week after Series 1 | 25 items; rated on a scale of 1-10 Lower score = better outcome Max = 10 per item; Max possible =250 overall Average across all valid responses Overall Score = Average\*10 Max of 19 items must be marked \>0 to be valid for tinnitus Subscores (each 3-4 items totaled) address 8 domains related to negative impact of tinnitus Intrusive, Sense of Control, Cognitive, Sleep, Auditory Difficulties, Relaxation, Quality of Life, and Emotional Distress |
| Secondary | Tinnitus Functional Index 2 | Change from Pre-Treatment Baseline to 1-Month after Series 1 | 25 items; rated on a scale of 1-10 Lower score = better outcome Max = 10 per item; Max possible =250 overall Average across all valid responses Overall Score = Average\*10 Max of 19 items must be marked \>0 to be valid for tinnitus Subscores (each 3-4 items totaled) address 8 domains related to negative impact of tinnitus Intrusive, Sense of Control, Cognitive, Sleep, Auditory Difficulties, Relaxation, Quality of Life, and Emotional Distress |
| Secondary | Tinnitus Functional Index 3 | Change from 1-Week to 1-Month after Series | 25 items; rated on a scale of 1-10 Lower score = better outcome Max = 10 per item; Max possible =250 overall Average across all valid responses Overall Score = Average\*10 Max of 19 items must be marked \>0 to be valid for tinnitus Subscores (each 3-4 items totaled) address 8 domains related to negative impact of tinnitus Intrusive, Sense of Control, Cognitive, Sleep, Auditory Difficulties, Relaxation, Quality of Life, and Emotional Distress |
| Secondary | Tinnitus Functional Index 4 | Change from Pre-Treatment Baseline to 1-Week after Series 2 | 25 items; rated on a scale of 1-10 Lower score = better outcome Max = 10 per item; Max possible =250 overall Average across all valid responses Overall Score = Average\*10 Max of 19 items must be marked \>0 to be valid for tinnitus Subscores (each 3-4 items totaled) address 8 domains related to negative impact of tinnitus Intrusive, Sense of Control, Cognitive, Sleep, Auditory Difficulties, Relaxation, Quality of Life, and Emotional Distress |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT04230577/registered?page=5