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The Impact of an Online Stress Management Program on In Vitro Fertilization (IVF) Outcome

The Impact of an Online Stress Management Program on IVF Outcome

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01156324
Enrollment
0
Registered
2010-07-02
Start date
2010-07-31
Completion date
2010-08-31
Last updated
2016-02-04

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

Conditions

Infertility

Keywords

IVF, Stress management

Brief summary

The goal of this study is to determine the impact of an online stress management program, which combines stress reduction and prevention strategies with personal care products/rituals which have relaxation properties, on pregnancy rates and psychological distress in women undergoing IVF for the first time.

Detailed description

The relationship between stress and infertility has remained a subject of controversy for many years. Recent research indicates that stress has a strong negative impact on pregnancy rates in women undergoing in vitro fertilization (IVF). In addition, stress is the most common reason given by women who voluntarily terminate treatment. In a recent study, women who participated in a group mind/body treatment program had higher pregnancy rates than control subjects. The impact of an online stress management program has never been studied in the infertile population. An online intervention would be far more accessible for many infertility patients.

Interventions

BEHAVIORALOnline Stress Management Group (Upliv)

Personalized online stress management program

BEHAVIORALControl

Control group receiving routine care along with $50 gift certificate at end of cycle

Sponsors

Boston IVF
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
21 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* female Boston IVF patients * day three FSH 12 or below * day three estradiol 80 pg/ml or below * able to read, understand and sign the informed consent in English * using own eggs (not egg donor) * willing and able to comply with study requirements * must be well versed in using a personal computer and the internet and must have access to an internet-connected computer seven days per week

Exclusion criteria

* prescription antipsychotic medication * previous diagnosis of borderline or narcissistic personality disorder * previous or concurrent participation in a mind/body group

Design outcomes

Primary

MeasureTime frameDescription
Clinical Pregnancy Rates1 yearClinical pregnancy rates will be recorded for IVF cycles 1 and 2.

Secondary

MeasureTime frameDescription
Psychological Status1 yearPsychological status is assessed by the following scales: Perceived Stress Scale (PSS), State Trait Anxiety Inventory (STAI), Beck Depression Inventory (BDI), Social Readjustment Scale (SRS), Daily Monitoring Form (DMF). Other than the DMF, these are all published validated scales.

Countries

United States

Outcome results

None listed

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