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

Status

Completed

Conditions

Intervention / Treatment

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.

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

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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