- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05444114
What Makes People Better at Describing Photographs?
August 15, 2024 updated by: Lori James, University of Colorado, Colorado Springs
This study is being conducted to learn more about how various personal and situational characteristics are related to the ability to provide verbal descriptions of photographs.
Participants will perform a brief mental exercise, then see three photographs with instructions to describe each thoroughly.
Participants will also complete several other surveys and measures.
Collected data will give researchers a better understanding of how different variables relate to speech production.
Study Overview
Detailed Description
This study is being conducted to learn more about how various personal and situational characteristics are related to the the ability to provide verbal descriptions of photographs.
Adult participants ages 18-30 and 65-80 will participate in videoconference calls during which they perform a brief mental exercise, then see three photographs with instructions to describe each thoroughly.
Descriptions are to be 30 to 60 seconds in length and are audio recorded for later scoring.
Participants will also complete several other surveys and measures, including some about anxiety, mindfulness, vocabulary, and demographics.
Participation will take approximately 40 to 60 minutes.
Collected data will be de-identified, and the aggregate data will give researchers a better understanding of how individuals' personality and cognitive traits and the mental exercise performed before the study relate to peoples' speech production performance.
Study Type
Interventional
Enrollment (Actual)
182
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Colorado
-
Colorado Springs, Colorado, United States, 80918
- UCCS
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- fluent speakers of English
- ages 18-30 or ages 65-80
Exclusion Criteria:
- non-fluent speakers of English
- people who are not ages 18-30 or ages 65-80
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Mindful Breathing
Participants follow instructions regarding a mindful breathing exercise on a 10-min audio clip
|
Participants perform a 10 minute mental exercise that is either mindful breathing or listening to a story
|
|
Active Comparator: Control
Participants follow instructions and listen to a 10-min audio clip of a story
|
Participants perform a 10 minute mental exercise that is either mindful breathing or listening to a story
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Speech Rate
Time Frame: During the 40 to 60 minute experimental session
|
Average number of words per second spoken
|
During the 40 to 60 minute experimental session
|
|
Speech Fillers Mid-Phrase
Time Frame: During the 40 to 60 minute experimental session
|
Average number of mid-phrase speech fillers as a percentage of words spoken
|
During the 40 to 60 minute experimental session
|
|
Speech Fillers Other
Time Frame: During the 40 to 60 minute experimental session
|
Average number of speech fillers not in the middle of a phrase as a percentage of words spoken
|
During the 40 to 60 minute experimental session
|
|
Repairs Plus False Starts
Time Frame: During the 40 to 60 minute experimental session
|
Average number of repairs plus false starts as a percentage of words spoken.
These two measures reflect the same underlying process so are summed together; indeed, one or the other term is sometimes used to indicate both measures.
|
During the 40 to 60 minute experimental session
|
|
Repetitions
Time Frame: During the 40 to 60 minute experimental session
|
Average number of repetitions as a percentage of words spoken
|
During the 40 to 60 minute experimental session
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Lori James, PhD, University of Colorado, Colorado Springs
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 22, 2022
Primary Completion (Actual)
May 23, 2023
Study Completion (Actual)
May 23, 2023
Study Registration Dates
First Submitted
June 18, 2022
First Submitted That Met QC Criteria
June 30, 2022
First Posted (Actual)
July 5, 2022
Study Record Updates
Last Update Posted (Actual)
August 22, 2024
Last Update Submitted That Met QC Criteria
August 15, 2024
Last Verified
August 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2020-006
- R15AG063111-01 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
De-identified participant data may be posted on a website for open access to other researchers, if the publication outlet requires it.,
but is not currently planned.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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