Contraception Clinical Trial
Official title:
A Pilot Study of the MyVoice:Rheum Decision Aid to Address the Reproductive Health Needs of Women With Rheumatic Diseases
Verified date | April 2024 |
Source | University of Pittsburgh |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This is a pilot trial to assess feasibility and acceptability of MyVoice:Rheum vs. a patient pamphlet among female patients ages 18-44 (n=40) who receive rheumatology care. • Hypothesis: MyVoice:Rheum will be feasible and acceptable to patients who receive rheumatology care.
Status | Completed |
Enrollment | 45 |
Est. completion date | March 1, 2023 |
Est. primary completion date | December 31, 2022 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 44 Years |
Eligibility | Inclusion Criteria: Patients must have at least one of four rheumatic diseases diagnosed by a rheumatologist: rheumatoid arthritis (RA), systemic sclerosis (SSc), myositis, Sjogren's syndrome, vasculitis, spondyloarthritis, and systemic lupus erythematosus (SLE). Patients must read and speak in English as a Spanish-language version of the tool has not yet been developed Access to a smart phone, personal computer, or tablet. Exclusion Criteria: - Women who have had prior hysterectomy or sterilization, or are pregnant. |
Country | Name | City | State |
---|---|---|---|
United States | UPMC Falk Rheumatology Clinic | Pittsburgh | Pennsylvania |
United States | UPMC Lupus Center of Excellence | Pittsburgh | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
University of Pittsburgh | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) |
United States,
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* Note: There are 31 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Reproductive Knowledge Assessment for Women With Rheumatic Diseases (ReproKnow) | Rheumatology-specific reproductive health knowledge was assessed via ReproKnow, a measure developed and preliminarily validated by our team that covers domains of contraception safety and efficacy, pregnancy management, pre-conception planning, medication safety, fertility; a score of nine indicates the highest level of reproductive knowledge | T2 (within 24 hours of intervention and appointment) compared to T0 (baseline) | |
Other | Perceived Efficacy in Patient-Physician Interactions | Self-reported efficacy in communicating with providers was assessed using a modified version of the validated five-item Perceived Efficacy in Patient-Provider Interactions (PEPPI) scale. Five-item measure with 5-point Likert scale questions from 1 (not at all confident) to 5 (very confident). Aggregate score is calculated by taking the individual item scores together and dividing by 5, with higher score indicating higher perceived efficacy in communicating with providers. | T2 (within 24 hours of intervention and appointment) compared to T0 (baseline) | |
Other | Participant Number of Pregnancies During Study | Assessed by participant-reported survey responses to a Yes/No item about whether a pregnancy has occurred since enrollment. | T3 (three months post-intervention) | |
Other | Quantity and Quality of Reproductive Health Conversation With Rheumatologist | Three-item measure. Did you talk to your rheumatologist about family planning today- yes/no; Did you make a decision related to family planning- yes/no; what was the family planning decision you made today? (Not Reported) | T2 (within 24 hours of intervention and appointment) | |
Primary | Acceptability of Intervention | Acceptability of Intervention Measure (AIM) consist of Four- item measure, Likert scales ranging from 1 (completely disagree) to 5 (completely agree). Score is determined by calculating the mean of scores, with a higher score indicating higher acceptability. We assigned a feasibility threshold of = 3.5 of 5, for which higher scores indicate more positive responses. | T2 (within 24 hours of intervention and appointment) | |
Primary | Intervention Appropriateness Measure | The validated Intervention Appropriateness Measure (IAM) consist of Four-item Likert scales ranging from 1 (completely disagree) to 5 (completely agree); we assigned a feasibility threshold of = 3.5 of 5 for IAM scores, for which higher scores indicate more positive responses. Score is determined by calculating the mean, with a higher score indicating greater appropriateness. | T2 (within 24 hours of intervention and appointment) | |
Primary | System Usability Scale | Usability was assessed via summary scores from the System Usability Scale (SUS), which consists of a 10-item Likert scale with scores ranging from 0-100; overall score calculated by finding the mean of items on scale. We set a threshold of scores >80.3 as 'A'/excellent and 68-80.3 as 'B'/very good, consistent with standard rating for the SUS. | T2 (within 24 hours of intervention and appointment) |
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