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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02607098
Other study ID # Pro00065075
Secondary ID
Status Completed
Phase N/A
First received November 13, 2015
Last updated February 28, 2017
Start date November 2015
Est. completion date November 2016

Study information

Verified date January 2017
Source Duke University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to understand the experience of men and their partners when diagnosed with male-factor infertility while trying to achieve a pregnancy and the skills they use to adapt to this diagnosis.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date November 2016
Est. primary completion date November 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion criteria:

Men:

- in a partnered relationship with a female

- have been trying without success to conceive a pregnancy

- have been referred due to suspected or diagnosed male-factor infertility

- have the ability to read and write English

Female Partner:

- 18 to 40 years of age

- ability to read and write English

Exclusion criteria:

- living children, either biological or adoptive

- history of vasectomy

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United Kingdom Newcastle Fertility Centre Newcastle-upon-Tyne England
United States Duke University Medical Center Durham North Carolina

Sponsors (1)

Lead Sponsor Collaborator
Duke University

Countries where clinical trial is conducted

United States,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Feasibility, as measured by the percentage of eligible subjects agreed to participate 6 months
Primary Feasibility, as measured by retention percentage 6 months
Secondary Change in level of global infertility stress, as measured by questionnaire Baseline, 6 months
Secondary Change in quality of life, as measured by questionnaire Baseline, 6 months
Secondary Change in level of global infertility stress, as measured by questionnaire The investigators will determine the change in pre and post significant event (when reported, such as new diagnosis, IVF/ICSI, discontinuation of treatment) level of global infertility stress in both the man and his partner. Pre and post significant event, up to 7 months
Secondary Change in quality of life, as measured by questionnaire The investigators will determine the change in pre and post significant event (when reported, such as new diagnosis, IVF/ICSI, discontinuation of treatment) level of quality of life in both the man and his partner. Pre and post significant event, up to 7 months
Secondary Concordance between men and partners with respect to levels of global infertility stress, as measured by questionnaire 3 months
Secondary Concordance between men and partners with respect to quality of life, as measured by questionnaire 3 months
Secondary Concordance between men and partners with respect to levels of global infertility stress, as measured by questionnaire 6 months
Secondary Concordance between men and partners with respect to quality of life, as measured by questionnaire 6 months
Secondary Feasibility, as measured by percentage of participants who used text messaging to complete their study questionnaires 6 months