None listed
Conditions
Brief summary
Aim The aim of this project is to determine if adults who stutter have superior quality of life (QOL), psychological well being, and speech functionality following 5 months access to an online social anxiety treatment for adults who stutter, known as iGlebe, compared to standard psychological services in the community. Objectives Primary objective: To compare quality of life with adults who stutter pre-treatment and 12 months post-treatment who have been randomly allocated to iGlebe or standard community practice, using the Overall Assessment of the Speaker's Experience of Stuttering (OASES). We are comparing the outcomes of participants from two groups: an online cognitive behaviour therapy program for social anxiety and standard psychological services in the community. Standard community care may consist of various service provisions, varying in cost, for example, private service providers or community health services. Participants in the standard care group can choose whichever option suits their individual circumstances. Secondary objectives: To measure levels of speech related anxiety and speech functionality pre-treatment and 12 months post-treatment for adults who stutter and who have been randomly allocated to iGlebe or standard psychological services in the community. Measures include self-reported stuttering severity, situation avoidance and a range of anxiety measures. Hypotheses 1. Participants who receive treatment with iGlebe will demonstrate significant improvements in Quality of life as measured by the Overall Assessment of the Speakers Experience of Stuttering (OASES), total score, at 12 months post randomisation compared to standard community services. 2. Participants who receive iGlebe will demonstrate significantly greater improvements in social anxiety than participants in the standard care group. 3. Participants who receive iGlebe will report significantly lower self-reported stuttering severity ratings than participants in the standard care group.
Interventions
This study is a randomised controlled trial investigating the quality of life, psychological benefits and speech outcomes of an online social anxiety treatment in comparison to standard clinical practice in the community for adults who stutter. Participants will be randomised to one of two groups: Online cognitive behaviour treatment or standard psychological services available in the community. The online cognitive behaviour treatment involves an internet program, known as iGlebe. The iGlebe program is a cognitive behaviour therapy program for social anxiety with people who stutter. The treatment is completely online without any input from live clinicians. iGlebe has seven modules. Participants complete the prescribed activities associated with each module before progressing to the next module. The first stage of the program involves developing an individualised profile for each participant. This is achieved by having the participant complete an online battery of assessments, The Unhelpful Thoughts and Beliefs About Stuttering scale, Avoidance of Speaking Situations questionnaire, The Fear of Negative Evaluation scale, and the Depression, Anxiety and Stress Scales. These assessments are designed to comprehensively identify destructive and irrational cognitions common to those who stutter, such as “people focus on every word I say,” “I won’t be able to keep a job if I stutter,” and “everyone in the room will hear me stutter.” The resultant profile is then used to design specific and individualised activities for each participant throughout the program. Instructions for each activity are given both in text on the screen and with pre-recorded spoken instructions from a psychologist with more than 20 years experience treating anxiety. Participants work through the activities at their own pace. Activities include behavioural experiments, cognitive restructuring, attention training, and writing tasks. Participants have access to iGlebe for 5 months. Research has shown this to be adequate time to complete the program. Participants work at their own pace through each of the modules. The time spent working through each module can vary depending on participant responses to the initial questionnaires and the time they spend working on the activities and tasks. Participants can choose to repeat tasks as well. It is recommended that participants log into the program at least weekly. The teaching components for each module is expected to take between 1 and 2 hours depending on the module. Adherence to iGlebe will be provided from data generated within the program and consists of dates of first login, date of login for each new module, date and page of last login.
Sponsors
Study design
Eligibility
Inclusion criteria
• 18 years and over • Formal diagnosis of stuttering by a speech pathologist via clinical interview over phone • Australian resident/citizen • Willingness to give written consent and willingness to participate and comply with the study.
Exclusion criteria
• Treatment for anxiety or depression from a mental health professional in the previous 12 months (not including assessment or less than 3 hours of contact) • Prior use of iGlebe in previous 12 months • Unwillingness or inability to stabilise prescribed psychological medication for duration of the trial • Risk of self-harm as assessed by the Beck Depression Inventory (such excluded participants will be referred for psychological care).