Family-focused therapy for individuals at high clinical risk for psychosis: A confirmatory efficacy trial.
Family-focused therapy for individuals at high clinical risk for psychosis: A confirmatory efficacy trial.
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DOI:
10.1111/eip.13208
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发表时间:
2022-06
影响因子:
2
通讯作者:
Bearden CE
中科院分区:
文献类型:
--
作者:
Miklowitz DJ;Addington JM;O'Brien MP;Denenny DM;Weintraub MJ;Zinberg JL;Mathalon DH;Cornblatt BA;Friedman-Yakoobian MS;Stone WS;Cadenhead KS;Woods SW;Sugar CA;Cannon TD;Bearden CE
Young people with attenuated psychotic symptoms (APS), brief intermittent psychosis, and/or genetic risk and functional deterioration are at high risk for developing psychotic disorders. In a prior trial, family-focused therapy for clinical high risk youth (FFT-CHR) was more effective than brief psychoeducation in reducing APS severity over 6 months. This 7-site trial will compare the efficacy of FFT-CHR to a psychoeducational and supportive intervention (enhanced care) on APS and social functioning in CHR individuals over 18 months. Participants (N = 220, ages 13–25 years) with a CHR syndrome will be randomly assigned to FFT-CHR (18 1-h sessions of family psychoeducation and communication/problem-solving skills training) or enhanced care (3 1-h family psychoeducational sessions followed by 5 individual support sessions), both given over 6 months. Participants will rate their weekly progress during treatment using a mobile-enhanced online platform. Family communication will be assessed in a laboratory interactional task at baseline and post-treatment. Independent evaluators will assess APS (primary outcome) and psychosocial functioning (secondary outcome) every 6 months over 18 months. We hypothesize that, compared to enhanced care, FFT-CHR will be associated with greater improvements in APS and psychosocial functioning over 18 months. Secondarily, improvements in family communication over 6 months will mediate the relationship between treatment condition and primary and secondary outcomes over 18 months. The effects of FFT-CHR are predicted to be greater in individuals with higher baseline risk for psychosis conversion. Results of the trial will inform treatment guidelines for individuals at high risk for psychosis.
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影响因子:
4.5
作者:
Addington J;Cadenhead KS;Cornblatt BA;Mathalon DH;McGlashan TH;Perkins DO;Seidman LJ;Tsuang MT;Walker EF;Woods SW;Addington JA;Cannon TD
通讯作者:
Cannon TD
影响因子:
5.9
作者:
Chambless, DL;Hollon, SD
通讯作者:
Hollon, SD
影响因子:
--
作者:
Charney, DS;Nemeroff, CB;Solomon, S
通讯作者:
Solomon, S
影响因子:
3.9
作者:
Benedict, RHB;Schretlen, D;Brandt, J
通讯作者:
Brandt, J
影响因子:
6.6
作者:
Ising, Helga K.;Kraan, Tamar C.;van der Gaag, Mark
通讯作者:
van der Gaag, Mark