Evaluation of a lifestyle program for improving fertility outcomes
Promoting ReprOductive WellbEing Through Shared Medical Appointments and Health Coaching Sessions
This study is testing a lifestyle program to see if it can help women aged 18-50 with fertility issues improve their health and fertility outcomes.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 55 (estimated) |
| Ages | 18 Years to 50 Years |
| Sex | Female |
| Sponsor | University Hospitals Cleveland Medical Center Academic / other |
| Locations | 1 site (Cleveland, Ohio) |
| Trial ID | NCT06297070 on ClinicalTrials.gov |
What this trial studies
This observational evaluation assesses the feasibility and acceptability of the Lifestyle Care for Fertility program, which includes integrative health consultations, shared medical appointments, and health coaching sessions. The program targets women aged 18-50 with fertility-related diagnoses and focuses on improving health behaviors and patient-reported outcomes through various wellness topics such as meditation, nutrition, and exercise. Data will be collected at multiple time points to track changes in health behaviors and outcomes over the course of the program.
Who should consider this trial
Good fit: Ideal candidates are women aged 18-50 with a fertility-related diagnosis who can participate in the Lifestyle Care for Fertility program.
Not a fit: Patients who are currently pregnant or have significant cognitive impairments may not benefit from this program.
Why it matters
Potential benefit: If successful, this program could enhance fertility outcomes and overall well-being for women facing fertility challenges.
How similar studies have performed: Other studies have shown promise in using lifestyle interventions to improve fertility outcomes, suggesting this approach may be beneficial.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult with a uterus aged from 18 to 50 years * Participating in the Lifestyle Care for Fertility program * Able to speak and understand English. * Has email address and access to mobile device with a functioning data plan. * Infertility-related diagnosis Exclusion Criteria: * Age \< 18 or \> 50 years * Having a significant and uncorrected visual, hearing, or cognitive impairment * Inability to provide consent * Current pregnancy
Where this trial is running
Cleveland, Ohio
- University Hospitals Cleveland Medical Center — Cleveland, Ohio, United States (Recruiting)
Study contacts
- Principal investigator: Christine Kaiser, DACM LAc — University Hospitals Cleveland Medical Center
- Study coordinator: Christine Kaiser, DACM LAc
- Email: Christine.Kaiser@UHhospitals.org
- Phone: (216) 285-4070
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.