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Group Psychotherapy for Patients With Hidradenitis Suppurativa: Effects in Quality of Life

Group Psychotherapy for Patients With Hidradenitis Suppurativa: Effects in Quality

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02904408
Enrollment
120
Registered
2016-09-19
Start date
2016-06-30
Completion date
2018-06-30
Last updated
2016-09-22

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

Conditions

Hidradenitis

Keywords

quality of life, psychotherapy, hidradenitis, treatments

Brief summary

The aim of this study is to determine the benefits of group psychotherapy on quality of life for people with hidradenitis suppurativa receiving medical and surgical treatment versus a control group (awaiting group) treated with medical and surgical treatment, without psychotherapy.

Detailed description

Further investigations studies are needed to determine the efficacy of psychological interventions for people with hidradenitis suppurativa. The aim of this study is to determine the benefits of group psychotherapy on quality of life for people with hidradenitis suppurativa receiving medical and surgical treatment versus a control group (awaiting group) treated with medical and surgical treatment, without psychotherapy. This is an experimental randomized trial with control group. Quality of life, symptoms: pruritus, odor and pain, distress and the illness will be measured before and after the intervention using psychological and quality of life questionnaires, and dermatological evaluations for 120 subjects. The investigators expect that the experimental group scores at the end of the psychotherapy program will be less than 4 points in Visual Analog Scale (VAS) for pruritus, odor and pain. The Dermatology Quality of Life Index (DQLI) expected to be less than 4 points from the initial score, and the patients are expected to present less than 7 points in Hospital Anxiety and Depression Scale (HADS). The experimental group scores will be less than the control group for quality of life, symptoms and distress.

Interventions

BEHAVIORALpsychotherapy

Group psychotherapy

Sponsors

Universitat Autonoma de Barcelona
CollaboratorOTHER
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Men and women at least 18 years old at the time of selection. * Subjects diagnosed with hidradenitis suppurativa. * Subjects that are in dermatological treatment. * Patients should be able to understand and communicate with the investigator.

Exclusion criteria

* Subjects suffering from a serious concomitant illness. * Subjects with a mental illness. * Subjects who are performing psychiatric treatment. * Subjects who are performing psychotherapy sessions both individual and group. * Patients who have alcohol dependence or drug abuse. * Subjects that present legal incapacity or limited legal capacity. * Subjects presenting illiteracy or language barriers.

Design outcomes

Primary

MeasureTime frameDescription
Dermatology Quality of Life Index (DLQI)1 yearThe Dermatology Life Quality Index or DLQI, developed in 1994, was the first dermatology-specific Quality of Life instrument. It is a simple 10-question validated questionnaire that has been used in over 40 different skin conditions in over 80 countries and is available in over 90 languages. Its use has been described in over 1000 publications including many multinational studies. The DLQI is the most frequently used instrument in studies of randomised controlled trials in dermatology.

Secondary

MeasureTime frameDescription
Hospital Anxiety and Depression Scale (HADS)1 yearHospital Anxiety and Depression Scale (HADS) was originally developed by Zigmond and Snaith (1983) and is commonly used by doctors to determine the levels of anxiety and depression that a patient is experiencing. The HADS is a fourteen item scale that generates ordinal data. Seven of the items relate to anxiety and seven relate to depression.
Hurley's staging system1 yearHurley separated patients into three groups based largely on the presence and extent of cicatrization and sinuses. It has been used as a basis for clinical trials in the past and is a useful basis to approach therapy for patients. These three stages are based on Hurley's staging system, which is simple and relies on the subjective extent of the diseased tissue the patient has. Hurley's three stages of hidradenitis suppurativa.
Visual analog scale (VAS) for pruritus1 yearA Visual Analogue Scale (VAS) is a measurement instrument that tries to measure a characteristic or attitude that is believed to range across a continuum of values and cannot easily be directly measured. Operationally a VAS is usually a horizontal line, 100 mm in length. The patient marks on the line the point that they feel represents their perception of their current state. The VAS score is determined by measuring in millimetres from the left hand end of the line to the point that the patient marks.
Visual analog scale (VAS) for pain1 yearA Visual Analogue Scale (VAS) is a measurement instrument that tries to measure a characteristic or attitude that is believed to range across a continuum of values and cannot easily be directly measured. Operationally a VAS is usually a horizontal line, 100 mm in length. The patient marks on the line the point that they feel represents their perception of their current state. The VAS score is determined by measuring in millimetres from the left hand end of the line to the point that the patient marks.
Visual analog scale (VAS) for odor1 yearA Visual Analogue Scale (VAS) is a measurement instrument that tries to measure a characteristic or attitude that is believed to range across a continuum of values and cannot easily be directly measured. Operationally a VAS is usually a horizontal line, 100 mm in length. The patient marks on the line the point that they feel represents their perception of their current state. The VAS score is determined by measuring in millimetres from the left hand end of the line to the point that the patient marks.
Hidradenitis Supurativa - Physician Global Assessment (HS-PGA)1 yearThe six-point Physician Global Assessment (PGA) ranges from clear to very severe. It is used in clinical trials to measure clinical improvement in inflammatory nodules, abscesses and draining fistulae.

Countries

Spain

Contacts

Primary ContactEsther Margarit de Miguel, Msc
emargarit@santpau.cat+34696617013
Backup ContactEva Vilarrasa, Dr
evilarrasa@santpau.cat+34935537007

Outcome results

None listed

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