ALSPAC – Age 7.5 – Phoneme Deletion Task
The Avon Longitudinal Study of Parents and Children (ALSPAC) assessed their cohort members (CMs) during the study’s age 7.5 sweep (Focus@7) using the Phoneme Deletion Task.
Details on this measure and the data collected from the CMs are outlined in the table below.
In this section
| Years of data collection: | 1998-2000 |
| Domain: | Verbal ability (language repetition) |
| Measures: | Spelling ability |
| Oral production and fluency | |
| Communication ability | |
| CHC: | Gc (Crystallised Intelligence) |
| Grw (Reading/Writing) | |
| CLOSER Source: | Explore this sweep in CLOSER Discovery: ALSPAC Childhood (5 years to 12 years 11 months) (opens in a new tab) |
| Administration method: | Trained interviewer; clinical setting; answers orally |
| Procedure: | Children were presented with a word, and then asked to repeat the word, and then say it again with part of the word missing, e.g. ‘sour’ without the ‘s’ = ‘our’. The task began with 2 practice trials, followed by 40 test trials, each of which increased in difficulty. The number of correctly spoken items was recorded. |
| Link to questionnaire: | http://www.bristol.ac.uk/alspac/researchers/our-data/clinical-measures/ (opens in new tab) |
| Scoring: | Correct items (0 – 40) |
| Item-level variable(s): | Not readily available |
| Total score/derived variable(s): | f7ws191 – f7ws220 Explore these variables in CLOSER Discovery: ALSPAC Focus at 7 Clinic Dataset (opens in a new tab) |
| Descriptives: | N = 8,074 |
| Range = 0 – 40 | |
| Mean = 20.05 | |
| SD = 9.53 | |
(click image to enlarge) |
|
| Age of participants (months): | Mean = 90.5 months, SD = 3.83, Range = 82 – 113 |
| Other sweep and/or cohort: | None |
| Source: | Rosner, J., & Simon, D. P. (1971). The auditory analysis test: An initial report. Journal of Learning disabilities, 4(7), 384-392. |
| Technical resources: | None |
| Example articles: | Powers, N. R., Eicher, J. D., Butter, F., Kong, Y., Miller, L. L., Ring, S. M., … & Gruen, J. R. (2013). Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment. The American Journal of Human Genetics, 93(1), 19-28. |
| Eicher, J. D., Powers, N. R., Miller, L. L., Mueller, K. L., Mascheretti, S., Marino, C., … & Pennington, B. F. (2014). Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ. Human Genetics, 133(7), 869-881. |
For the named items in the table above, links are provided to their corresponding content on CLOSER Discovery. Where a variable range is provided, full variable lists can be accessed through the ‘Variable Groups’ tab on the linked Discovery page.