Double ABCX Theory Based Cognitive Psychotherapy Combined Progressive Muscle Relaxation Intervention on Women Undergoing IVF-ET
Primary Purpose
Infertility
Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Cognitive progressive muscular relaxation therapy
Sponsored by
About this trial
This is an interventional supportive care trial for Infertility focused on measuring cognitive psychotherapy, progressive muscular relaxation, in vitro fertilization and embryo transfer(IVF-ET), Couples Therapy
Eligibility Criteria
Inclusion Criteria:
- The couple who are eligible for in vitro fertilization-embryo transfer (IVF-ET) treatment;
- Junior high school and above;
- voluntarily accepted for investigation and signed informed consent.
Exclusion Criteria:
- Suffering from physical diseases such as severe heart, liver and kidney, and mental disorders;
- Experiencing major traumatic events in the past 2 years.
Sites / Locations
- Infertility Reproductive Center, Second Xiangya Hospital, Central South University
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
No Intervention
Arm Label
Women intervention arm
Couple intervention arm
Control arm
Arm Description
Intervention will be applied to the women within the couple.
Intervention will be applied to the couple, both men and women.
The couple will receive the normal nursing care.
Outcomes
Primary Outcome Measures
Change of depression score
The Self-reported Depression Scale (SDS)will be used to assess the score of depression.The total score of SDS ranges from 0-80, with 40 as the cutoff. The higher the total score, the more depressive.
Change of anxiety score
The Self-reported Anxiety Scale (SAS) will be used to assess the score of anxiety.The total score of SAS ranges from 0-80, with 30 as the cutoff. The higher the total score, the more anxious.
Secondary Outcome Measures
Change of Blood Cortisol
This is a kind of hormone closely related to stress, and the investigators will measure the level of Blood Cortisol by Blood test.
Change of sleeping quality
The physical condition closely related to stress. The investigators will use Self-Rating Scale of Sleep to measure the sleeping quality of the participants. The total sore ranges from 5 to 50, with higher score reflects better sleep quality.
Successful conception rate (%)
The investigators will count the successful conception rate at each arms.
Full Information
NCT ID
NCT03931187
First Posted
April 23, 2019
Last Updated
November 30, 2021
Sponsor
Central South University
1. Study Identification
Unique Protocol Identification Number
NCT03931187
Brief Title
Double ABCX Theory Based Cognitive Psychotherapy Combined Progressive Muscle Relaxation Intervention on Women Undergoing IVF-ET
Official Title
Double ABCX Theory Based Cognitive Psychotherapy Combined Progressive Muscle Relaxation Intervention on Women Undergoing In Vitro Fertilization-Embryo Transfer Treatment
Study Type
Interventional
2. Study Status
Record Verification Date
November 2021
Overall Recruitment Status
Completed
Study Start Date
December 1, 2018 (Actual)
Primary Completion Date
May 1, 2019 (Actual)
Study Completion Date
July 1, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Central South University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The in vitro fertilization and embryo transfer(IVF-ET) is a therapy to help the infertile couples. The mental health status of couple under IVF-ET, commonly seen in depression and anxiety, is found to be closely related to the success of IVF-ET. This study aims to develop a intervention program combing cognitive psychotherapy and progressive muscle relaxation to ease the negative emotion and promote the success rate among couples undergoing IVF-ET.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility
Keywords
cognitive psychotherapy, progressive muscular relaxation, in vitro fertilization and embryo transfer(IVF-ET), Couples Therapy
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
67 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Women intervention arm
Arm Type
Experimental
Arm Description
Intervention will be applied to the women within the couple.
Arm Title
Couple intervention arm
Arm Type
Experimental
Arm Description
Intervention will be applied to the couple, both men and women.
Arm Title
Control arm
Arm Type
No Intervention
Arm Description
The couple will receive the normal nursing care.
Intervention Type
Behavioral
Intervention Name(s)
Cognitive progressive muscular relaxation therapy
Intervention Description
This therapy combines cognitive psychotherapy and progressive muscular relaxation, intervened 6 times with 1-1.5 hour each time. The whole therapy will last round 28-30 days during IVF-ET.
Primary Outcome Measure Information:
Title
Change of depression score
Description
The Self-reported Depression Scale (SDS)will be used to assess the score of depression.The total score of SDS ranges from 0-80, with 40 as the cutoff. The higher the total score, the more depressive.
Time Frame
The investigators will measure the socre of depression at baseline and immediately after intervention ( the duration of intervention is around 1 month).
Title
Change of anxiety score
Description
The Self-reported Anxiety Scale (SAS) will be used to assess the score of anxiety.The total score of SAS ranges from 0-80, with 30 as the cutoff. The higher the total score, the more anxious.
Time Frame
The investigators will measure the socre of anxiety at baseline and immediately after intervention ( the duration of intervention is around 1 month).
Secondary Outcome Measure Information:
Title
Change of Blood Cortisol
Description
This is a kind of hormone closely related to stress, and the investigators will measure the level of Blood Cortisol by Blood test.
Time Frame
The investigators will measure the socre of Blood Cortisol at baseline and immediately after intervention ( the duration of intervention is around 1 month).
Title
Change of sleeping quality
Description
The physical condition closely related to stress. The investigators will use Self-Rating Scale of Sleep to measure the sleeping quality of the participants. The total sore ranges from 5 to 50, with higher score reflects better sleep quality.
Time Frame
The investigators will measure the socre of sleeping quality at baseline and immediately after intervention ( the duration of intervention is around 1 month).
Title
Successful conception rate (%)
Description
The investigators will count the successful conception rate at each arms.
Time Frame
The doctor will test whether it is successfully conceived 4 weeks after the embryo is implanted. The last intervention is on the day of embryo implantation. The investigators will count this 4 weeks after completion of intervention.
10. Eligibility
Sex
All
Gender Based
Yes
Gender Eligibility Description
Biological sex
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
The couple who are eligible for in vitro fertilization-embryo transfer (IVF-ET) treatment;
Junior high school and above;
voluntarily accepted for investigation and signed informed consent.
Exclusion Criteria:
Suffering from physical diseases such as severe heart, liver and kidney, and mental disorders;
Experiencing major traumatic events in the past 2 years.
Facility Information:
Facility Name
Infertility Reproductive Center, Second Xiangya Hospital, Central South University
City
Changsha
State/Province
Hunan
ZIP/Postal Code
410013
Country
China
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
The participants are not willing to share the data.
Learn more about this trial
Double ABCX Theory Based Cognitive Psychotherapy Combined Progressive Muscle Relaxation Intervention on Women Undergoing IVF-ET
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