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Internet-based Emotion Regulation Intervention for Sexual Health

SHER 2: Internet-delivered Emotion Regulation Skills Training for Sexual Health: a Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04792177
Acronym
SHER2
Enrollment
62
Registered
2021-03-10
Start date
2021-05-05
Completion date
2022-07-30
Last updated
2022-11-14

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

Conditions

Sexual Dysfunction, Sexual Dysfunctions, Psychological

Keywords

internet intervention, emotion regulation, sexual health

Brief summary

Introduction: Emotion regulation difficulties have been associated with mental disorders and sexual dysfunctions. Traditional face-to-face transdiagnostic emotion regulation interventions have shown positive results for emotional and personality disorders. Only recently have the effects of these interventions on sexual health started to be investigated. Internet-delivered psychological interventions have several advantages over face-to-face interventions, such as cost-effectiveness, accessibility and suitability for people who experience shame because of their stigmatized problematic behaviors and those who avoid seeking help. The aims of the SHER 2 study are: a) determine the efficacy of an Internet-based emotion regulation intervention for sexual health and sexual satisfaction, and; b) explore the effects of the intervention on (1) emotion regulation skills; (2) mental health; (3) sexual self-perception.

Interventions

The intervention will involve an online emotion-regulation skills training for individuals with sexual problems. It will last for 8 weeks, encompassing psycho-educational and emotion-regulation skills components. Every week participants will gain access to a different intervention module of the training, containing videos, presentation slides, written support material and a recommendation of activities to be completed until the following week of training. Participants are expected to dedicate 30 minutes to one hour per week to complete each module.

Sponsors

Luxembourg National Research Fund (FNR)
CollaboratorUNKNOWN
Linkoeping University
CollaboratorOTHER_GOV
University of Lausanne
CollaboratorOTHER
University of Luxembourg
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Participants are assigned to one of two groups for the duration of the study. 50% of participants will be assigned to the intervention group while the other 50% will be assign to a waitlist control condition. The waitlist group will have access to the intervention after 6 months.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* between 18 and 65 years of age, * fluent in Brazilian Portuguese, * self-reported sexual problems, assessed in men by a score of \< 21 on the International Index Erectile Function (IIEF) and in women by a score of \< 26 on the Female Sexual Function Index (FSFI), * in a stable relationship for at least the preceding 3 months.

Exclusion criteria

* medical conditions that can interfere with the outcomes of the intervention, e.g., diabetes, cancer, cardiovascular problems, * ongoing psychotherapy. * no sexual activity in the previous 4 weeks.

Design outcomes

Primary

MeasureTime frameDescription
Change in Female Sexual Function Index (FSFI) at 6 monthsbaseline, 2 months after baseline (end of intervention), 8 months after baseline (follow-up)this is a 19-item questionnaire for the assessment of sexual functioning in women in domains of sexual functioning (e.g., sexual arousal, orgasm, satisfaction, pain). Answers are provided using a 5-point Likert scale.
Change in International Index of Erectile Function (IIEF)at 6 monthsbaseline, 2 months after baseline (end of intervention), 8 months after baseline (follow-up)The IIEF is 15-item, self-administered questionnaire for assessing sexual functioning in men. Answers are given on a 6-point Likert scale. The IIEF encompasses five different domains of sexual functioning: erectile function, orgasm function, sexual desire, intercourse satisfaction and overall satisfaction.
Change in Sexual Quotient (QS) at 6 monthsbaseline, 2 months after baseline (end of intervention), 8 months after baseline (follow-up)The QS is a brief and comprehensive tool composed of 10-questions, which are answered on a scale from 0 (never) to 5 (always). It addresses general sexual function, and stages of the sexual response cycle (desire, arousal, orgasm) and sexual satisfaction.

Secondary

MeasureTime frameDescription
General Anxiety Disorder - 7 (GAD-7)baseline, 2 months after baseline (end of intervention), 8 months after baseline (follow-up)A 7-item self-report measure used to assess symptoms of anxiety.
Sexual Modes Questionnaire (SMQ) - Automatic Thoughts subscalebaseline, 2 months after baseline (end of intervention), 8 months after baseline (follow-up)This self-report scale consists of 30 items in the male version, and 33 items in the female version. Respondents are asked to rate the frequency (from 1 \[never\] to 5 \[always\]) with which they have experienced specific automatic thoughts during sexual activity.
the Difficulties in Emotion Regulation Scale (DERS)baseline, 2 months after baseline (end of intervention), 8 months after baseline (follow-up)The DERS assesses several facets of emotion regulation, including difficulties relevant to an individual's (a) acceptance of emotional responses, (b) ability to engage in goal-directed behaviour under distress, (c) ability to control impulsive behaviours when distressed, (d) access to emotion regulation strategies, and (e) emotional clarity. Participants rate their degree of agreement with each statement on a scale from 1 (almost never; 0 to 10 percent) to 5 (almost always; 91 to 100 percent).
Sexual Self-Schema Scale (SSSS).baseline, 2 months after baseline (end of intervention), 8 months after baseline (follow-up)consists of 30 items assessing respondents' perception of themselves as a sexual person compared to others of the same gender and age. Answers are provided using a 5- point Likert scale ranging from 1 (not at all descriptive of me) to 5 (very much descriptive of me).
Patient Health Questionnaire-9 (PHQ-9)baseline, 2 months after baseline (end of intervention), 8 months after baseline (follow-up)A 9-item self-report measure used to assess symptoms of depression.

Countries

Luxembourg

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026