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Needs Assessment Evaluating Quality of Life Issues for Gastroparesis Patients and Caregivers

Needs Assessment Evaluating Quality of Life Issues for Gastroparesis Patients and Caregivers

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01329211
Enrollment
68
Registered
2011-04-05
Start date
2010-01-31
Completion date
2013-02-28
Last updated
2013-05-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastroparesis

Keywords

Gastroparesis, Quality of Life

Brief summary

The project will involve conducting a Needs Assessment for Gastroparesis patients and their caregivers with the goal of identifying quality of life issues associated with this disease. Identifying these issues will ameliorate management and support systems for gastroparesis currently existent in the community and, hopefully, provide information for the establishment of more resources to assist the patients and their families.

Detailed description

This project will involve: a) distributing questionnaires to up to 200 participants (100 patients and 100 caregivers) at the Shands Gastrointestinal clinic and b) focus groups including patients, medical provider, and the clinic case manager. The questionnaires will provide information on the relative effect of gastroparesis on the quality of life of the patients and their caregivers. Assessment of this needs assessment will then help identify areas of potential resource improvement and mobilization to provide support for the patients and their family members.

Interventions

None listed

Sponsors

University of Florida
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Gastroparesis patients at the GI clinic of Shands Hospital at the University of Florida * Caregivers to Gastroparesis patients at the GI clinic of Shands Hospital at the University of Florida

Exclusion criteria

* Inability to fill out the questionnaires by any cause

Design outcomes

Primary

MeasureTime frame
Score in a Quality of life assessment QuestionnaireDuring the clinicial visit at the day of enrollment(Day 1)

Secondary

MeasureTime frame
Score in a Quality of life assessment Questionnaire1st follow-up, at 6 months from Date of enrollment

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026