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. 2012 Aug 15;2012(8):CD005652. doi: 10.1002/14651858.CD005652.pub2

Morey 2010.

Study characteristics
Methods design: parallel‐arm, randomised controlled trial
Participants sex: 13/16 females (81.3%)
age: mean age 31.1 years
location: USA
setting: outpatient
exclusions: active psychosis, history of schizophrenia, substance intoxication or withdrawal
level of functioning/severity of illness: no further information
BPD diagnosis according to: DSM‐IV
means of assessment: DIPD‐IV, PAI‐BOR
Interventions group 1: MACT (6 weekly sessions centred on chapters of a patient workbook)
group 2: MACT+TA (6 weekly sessions centred on chapters of a patient workbook; initial session also included an individualised collaborative assessment with development of questions the client would like to "ask the test data" about themselves and the articulation of specific, individualised treatment goals; during second session, therapist and client discussed assessment results and motivational feedback was given; apart from these augmentations of the first two sessions, identical treatment as other group
duration: 1,5 months
concomitant psychotherapy: no other psychosocial interventions allowed
concomitant pharmacotherapy: psychotropic medication allowed 56% were taking at baseline
Outcomes outcomes considered in this review
self‐rated:
observer‐rated: BPD severity (PAI‐BOR‐total), affective instability (PAI‐BOR‐A), suicidality (PAI‐BOR‐SI), parasuicidality (PAI‐BOR‐S), interpersonal problems (PAI‐BOR‐N), identity disturbance (PAI‐BOR‐I)
time‐points used here: 1,5 months (i.e. post‐treatment)
Notes analyses: ITT (completers case analysis also available but not used here)
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Unclear risk Unclear
Allocation concealment (selection bias) Unclear risk Unclear
Blinding of outcome assessment (detection bias)
All outcomes Unclear risk "[...] assessments [...] were conducted by an independent evaluator" (Morey 2010, p. 533)
Selective reporting (reporting bias) Unclear risk No indication for selective reporting, but Insufficient information to permit judgement of 'Yes' or 'No'.
Treatment adherence? Low risk "Consenting clients in both conditions were assigned to a project therapist, who worked under the supervision of the primary investigator." (Morey 2010, p. 532)
Allegiance effect improbable? Low risk No indication given.
Attention bias: equal amounts of attention to all groups (obligatory treatment components)? Low risk Beyond TA (which was the point of question of the trial), both groups received comparable amounts of attention.