Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
6 participants
INTERVENTIONAL
2009-06-30
2009-10-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The study will look at the issues involved in setting up a large-scale investigation of treatment for young people who stammer. It will inform the investigators whether larger studies would be possible and give some early-stage information on the effectiveness of group SALT for these young people. The findings will pave the way for building and testing out treatment programmes where there will be clear positive benefit for young people who stammer and their families.
To answer the research question, the study will tell the investigators (a) how easy/difficult it was to get people to take part, (b) young people and parents'/carers' views on taking part and (c) whether the assessments were able to pick up changes in speech and attitudes towards stammering reported by the young people and their carers.
Sufficient numbers of participants were not recruited to carry out the intended rehearsal pilot RCT study design.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Comparative Study Between Three Different Methods for Stuttering Therapy in Children
NCT05291572
Stimulation of the Thalamus to Ameliorate Persistent Disfluency
NCT05641701
Modifying Unconscious Tongue Movements in Adults With Developmental Stammer.
NCT04310436
Spacing Lidcombe Program Clinic Visits
NCT00680303
Auditory Prediction and Error Evaluation in the Speech of Individuals Who Stutter
NCT06181149
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
SINGLE_GROUP
HEALTH_SERVICES_RESEARCH
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Treatment group
attendance at one-week speech therapy group
One-week speech therapy group
One-week cross-district speech therapy group for older children (aged 8 to 15) who stammer
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
One-week speech therapy group
One-week cross-district speech therapy group for older children (aged 8 to 15) who stammer
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Currently in treatment, on review or on waiting list for treatment.
* Has had an initial NHS Speech and Language Therapy assessment by Newcastle, Northumberland or North Tyneside Speech and Language Therapy service.
* Has a diagnosis of stammering.
* Has sufficient understanding of spoken (English) language to score at or above the 16th percentile on the Understanding Linguistic Concepts subtest of the CELF-4UK assessment.
* Available to attend treatment for the whole week of 20th July 2009
* Available to attend treatment for the whole week of 24th August 2009
Exclusion Criteria
* Diagnosis of moderate or severe general learning difficulties
* Diagnosis of moderate or severe receptive and/or pragmatic language difficulties
* Parent/carer for whom an interpreter would be required
8 Years
15 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Newcastle Upon-Tyne
OTHER
North Tyneside Primary Care Trust
UNKNOWN
Northumberland Care Trust
UNKNOWN
Newcastle-upon-Tyne Hospitals NHS Trust
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Lucy E Paterson, MA, BSc
Role: PRINCIPAL_INVESTIGATOR
Newcastle upon Tyne NHS Hospitals Foundation Trust
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Newcastle-upon-Tyne Hospitals NHS Trust
Newcastle upon Tyne, Tyne and Wear, United Kingdom
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
4565
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.