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Completed

NCT Number: NCT04024670

The Impact of Arts-Based Interventions on Patient Hospital Experience

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Key information

Conditions

High Risk Pregnancy Bone Marrow

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Alabama at Birmingham

Birmingham, Alabama, 35233, United States

About this study

interventions and timing of interventions

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion:

  • Inpatient on either Bone Marrow Transplant ICU or High Risk Obstetrics Unit
  • Estimated length of stay 2 or more weeks
  • Age >18
  • Patients who will potentially benefit from the AIM experience

Additional Inclusion Criteria:

  • For the High Risk Obstetrics Unit group (hand-sewing), patients should be physically able to participate in hand-sewing activity.
  • For the Bone Marrow Transplant IUC group (story-telling/poetry), patients should be physically able to participate in story-telling/poetry activity.

Exclusion:

  • Patient too ill
  • Complex medical condition that requires therapies which would not allow time for participation
  • Declined to participate
  • Age <18

Treatment and study plan

Arts Intervention

Other

If selected for the arts activity, an artist in residence will visit you 3 times a week for a total of 3 weeks during your hospital stay. Two visits will focus on the arts activity and one visit will be the administration of the questionnaire. Each visit will be approximately 25 minutes at a time.

Primary outcomes

  1. Evaluate patient experience during the course of intervention using name of survey

    Time frame: Baseline at admissions

    define survey - evaluate experiences, range of survey - explain likert scale 0-10 with 0 being x (allows patient to rate how much they disagree or agree with a statement), 0 being the worst outcome and 10 being the best

  2. Evaluate patient experience during the course of intervention using name of survey

    Time frame: Baseline - end of week 1

    define survey - evaluate experiences, range of survey - explain likert scale 0-10 with 0 being x (allows patient to rate how much they disagree or agree with a statement), 0 being the worst outcome and 10 being the best

  3. Evaluate patient experience during the course of intervention using name of survey

    Time frame: week 1- week 2

    define survey - evaluate experiences, range of survey - explain likert scale 0-10 with 0 being x (allows patient to rate how much they disagree or agree with a statement), 0 being the worst outcome and 10 being the best

  4. Evaluate patient experience during the course of intervention using name of survey

    Time frame: week 2 - week 3

    define survey - evaluate experiences, range of survey - explain likert scale 0-10 with 0 being x (allows patient to rate how much they disagree or agree with a statement), 0 being the worst outcome and 10 being the best

  5. Evaluate patient experience during the course of intervention using name of survey

    Time frame: week 3 - weekly up to 10 weeks

    define survey - evaluate experiences, range of survey - explain likert scale 0-10 with 0 being x (allows patient to rate how much they disagree or agree with a statement), 0 being the worst outcome and 10 being the best

Sponsors and collaborators

Lead sponsor

University of Alabama at Birmingham

Other

Registry information

Official study title

The Impact of Arts-Based Interventions on Patient Hospital Experience for Patients on a High-Risk Obstetrics and Bone Transplant Units

Important dates

Study start
2019
Primary completion
2023
Study completion
2023
First posted
Jul 18, 2019
Registry last updated
Jul 10, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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