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Graded Exposure Therapy in Chronic Pelvic Pain

U

University of Granada (UGR)

Status

Unknown

Conditions

Chronic Pelvic Pain

Treatments

Other: Physiotherapy
Other: Graded exposure therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT03590236
DF0069UG

Details and patient eligibility

About

Chronic pelvic pain (CPP) is considered as nonmalignant recurrent or continuous pain related to the structures of the pelvis. The objective of this study was to evaluate the effects of graded exposure therapy in women with chronic pelvic pain.

Full description

Chronic pelvic pain (CPP) is considered as nonmalignant recurrent or continuous pain related to the structures of the pelvis. This condition lasts at least 6 months, and many times is associated with negative cognitive, emotional, sexual and behavioral consequences.In addition to the high economic cost, CPP is also costly in emotional and psychological suffering. This clinical trial aims to evaluate the effects of a program based on graded exposure therapy in women with chronic pelvic pain.

Enrollment

60 estimated patients

Sex

Female

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of chronic pelvic pain
  • Moderate fear of movement

Exclusion criteria

  • Other clinical diagnosis.
  • Men
  • Other pathology such as neurological disease.
  • Cognitive impairment.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

60 participants in 3 patient groups

Graded exposure therapy
Experimental group
Description:
Patients in this group received graded exposure therapy added to physiotherapy
Treatment:
Other: Graded exposure therapy
Physiotherapy
Active Comparator group
Description:
Patients included in this group received the standard treatment based on a physiotherapy approach.
Treatment:
Other: Physiotherapy
Control group
No Intervention group
Description:
Waiting list patients

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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