Using patient-chosen visual art to improve hospital satisfaction during pregnancy admissions
Randomized Control Trial: Impact of Patient Selected Visual Art in the Hospital Room During Antepartum Admission on Hospital Satisfaction Scores and Patient Experience.
This study tests if letting pregnant patients choose the artwork in their hospital room can make them feel happier and more satisfied during their stay.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 100 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | Albany Medical College Academic / other |
| Locations | 1 site (Albany, New York) |
| Trial ID | NCT06790043 on ClinicalTrials.gov |
What this trial studies
This study evaluates the impact of allowing patients to select visual art for their hospital room during antepartum admissions. By comparing patient satisfaction scores between those who choose their art and those who receive routine care, the study aims to determine if personalized visual elements can enhance the overall hospital experience. The methodology involves collecting satisfaction data through questionnaires administered to participants during their stay. The focus is on improving the emotional and psychological well-being of pregnant patients in a hospital setting.
Who should consider this trial
Good fit: Ideal candidates for this study are pregnant women aged 18 and older who are admitted to the antepartum unit at the study hospital.
Not a fit: Patients who are under 18, not pregnant, or unable to provide informed consent in English will not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance patient satisfaction and overall experience during hospital stays for pregnant women.
How similar studies have performed: While the specific approach of patient-selected visual art is novel, similar studies have shown that personalized environments can improve patient satisfaction in healthcare settings.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * patients who are greater than or equal to 18 years of age * patients admitted to the study hospital's antepartum unit for care * currently pregnant * willing and able to provide informed consent and complete the provided questionnaire Exclusion Criteria: * patients less than 18 years of age * patients who are not pregnant * patients who are not admitted to study hospital's antepartum unit * patients who cannot provide informed consent in English * patients who have participated in this study during a previous admission
Where this trial is running
Albany, New York
- Albany Medical Center — Albany, New York, United States (Recruiting)
Study contacts
- Principal investigator: Scott Dexter, MD — Albany Medical College
- Study coordinator: Scott Dexter, MD
- Email: dexters@amc.edu
- Phone: 518-262-5182
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.