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Cognitive behavioral therapy to improve quality of life after surgical treatment of women with endometriosis

Completed
Conditions
The presence of endometrium like tissue outside the wobe
10038612
10052863
Registration Number
NL-OMON52725
Lead Sponsor
Rijnstate Ziekenhuis
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
100
Inclusion Criteria

Age: 18 to 50 years
Proven endometriosis (by ultrasound, MRI or surgery)
An indication for endometriosis debulking surgery due to endometriosis-related
pain
Being able to understand, read and write Dutch

Exclusion Criteria

An mood, anxiety or personality disorder diagnosis according to the DSM-5 at
the moment of inclusion
Undergoing psychological treatment at the moment of inclusion
Use of psychopharmacologic medication aimed at altering mood at the moment of
inclusion
Patients that have endometriosis-related unwanted childlessness only
Scalp hair shorter than 4 cm

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The primary objective of this study is to investigate whether usual care<br /><br>combined with CBT improves QoL in patients undergoing surgery for endometriosis<br /><br>compared to usual care only.</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>Secondary objectives are to investigate whether pain intensity, pain<br /><br>cognitions, perceived stress and objectively measured cortisol levels mediate<br /><br>the effects of CBT on QoL in both groups.</p><br>
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