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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05299983
Other study ID # 140604
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date January 15, 2022
Est. completion date March 31, 2022

Study information

Verified date March 2022
Source University of California, San Diego
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

As part of a National Institute on Aging -funded R01, the investigators developed an evidence-based, multi-media digital resource entitled MyMenoPlan to help women learn about the menopause transition, and the symptoms and treatments of perimenopause/menopause. MyMenoPlan is also designed to help women learn about the effectiveness of treatments for a comprehensive list of midlife symptoms and compare treatments that may help with the specific symptoms women are experiencing.


Description:

The purpose of this research study is to: 1. Investigate how women randomly assigned to visit MyMenoPlan use the website (time spent on website, treatment and symptom page views, use of interactive tools, and use of the MyMenoPlan tool). 2. Compare the ratings of women randomly assigned to MyMenoPlan to those randomly assigned to other menopause websites for perceived quality of information, readability, self-efficacy, and credibility of these online menopause resources.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 410
Est. completion date March 31, 2022
Est. primary completion date March 31, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 40 Years to 60 Years
Eligibility Inclusion Criteria: - As stated above Exclusion Criteria: - N/A

Study Design


Related Conditions & MeSH terms


Intervention

Other:
MyMenoPlan
Participants are asked to spend at least 20 minutes on the website (MyMenoPlan) assigned to them.
Control
Participants are asked to spend at least 20 minutes on at least one of the following websites: North American Menopause Society: https://www.menopause.org/for-women National Institute on Aging: https://www.nia.nih.gov/health/topics/menopause The Office on Women's Health-Menopause: https://www.womenshealth.gov/menopause

Locations

Country Name City State
United States UC San Diego La Jolla California

Sponsors (1)

Lead Sponsor Collaborator
University of California, San Diego

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Perceived Quality of Information This 7-item, 5-point Likert scale (1- Strongly disagree to 5 - Strongly agree) is adapted from the Post-Study System Usability Questionnaire (PSSUQ) in Lewis (1995).
Items:
Reading the information made me feel in more control of my perimenopause/menopause.
The information on the website(s) was helpful to me.
I found the information I was looking for.
The information answered my questions about perimenopause/menopause.
I liked the website (s).
I would have liked more in-depth information. (reverse-coded)
The website(s) were fairly comprehensive about perimenopause /menopause.
Each survey question is answered after spending at least 20 minutes on the assigned website(s)
Primary Readability This 2-item, 5-point Likert (1- Strongly disagree to 5 - Strongly agree)scale was derived from the Standardized User Experience Percentile Rank Questionnaire (SUPR-Q) in Sauro (1995).
Items:
The information I read was clear.
The information I read was easy for me to understand.
Each survey question is answered after spending at least 20 minutes on the assigned website(s)
Primary Self-Efficacy for Managing Menopause Symptoms This is a newly developed Likert scale (1- Strongly disagree to 5 - Strongly agree) for assessing participants' beliefs in their own abilities in managing menopausal symptoms.
Items:
If I want to, I am certain I could figure out the treatments or coping strategies that would work best for me.
I feel I could treat or cope with my symptoms of perimenopause/menopause if I want to.
Each survey question is answered after spending at least 20 minutes on the assigned website(s)
Primary Credibility This 2-item, 5-point Likert (1- Strongly disagree to 5 - Strongly agree) scale was derived from the Standardized User Experience Percentile Rank Questionnaire (SUPR-Q) in Sauro (1995).
Items:
The information is credible.
The information is trustworthy.
Each survey question is answered after spending at least 20 minutes on the assigned website(s)
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