Assisted reproductive technology
Conditions
Interventions
Observer group:The implementation of spouse synchronous cognitive therapy
Control group:Implementation of usual care
Sponsors
Women' s Hospital, School of Medicine, Zhejiang University, Hangzhou
Eligibility
Sex/Gender
All
Age
20 Years to 40 Years
Inclusion criteria
Inclusion criteria: Patient inclusion criteria: (1) Women aged 20-40 years; (2) Identified as infertility caused by female factors, and registered to first IVF treatment; (3) Junior high school and above education level, can read and understand Chinese, no communication barriers ; (4) Clear consciousness; (5) Voluntary participation in this study; (6)Living with spouses, patients and spouses can cooperate with the researchers to complete each stage of health education related content. Spouse inclusion criteria: (1)as the main caregivers ; (2)Junior high school and above education level, can read and understand Chinese, no communication barriers ; (3)Consciousness is clear, no serious medical and surgical history of mental illness.
Exclusion criteria
Exclusion criteria: Patient exclusion criteria : (1) Exclusion of chromosomal abnormalities or other serious genetic diseases. (2) Patients had severe physical illness or drug dependence; (3) Other negative life events occurred in the same period; (4) To participate in other clinical trials or psychological intervention researchers; (5) Accompanied by other diseases which seriously affect the quality of life, such as heart, cerebrovascular etc. (6) Researchers believe that other reasons are not suitable for clinical researchers. Spouse exclusion criteria : (1) Exclusion of chromosomal abnormalities or other serious genetic diseases. (2) Patients had severe physical illness or drug dependence; (3) Other negative life events occurred in the same period; (4) To participate in other clinical trials or psychological intervention researchers; (5) Accompanied by other diseases which seriously affect the quality of life, such as heart, cerebrovascular etc. (6) Researchers believe that other reasons are not suitable for clinical researchers.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Dyadic Coping Inventory;Fertility Quality of Life Questionnaire; | — |
Secondary
| Measure | Time frame |
|---|---|
| General Self-Efficacy Scale;SPWB-Autonomy; | — |
Countries
China
Contacts
Public ContactMaqing
Women' s Hospital, School of Medicine, Zhejiang University, Hangzhou
Outcome results
None listed