Demographic description of the participants at randomization.

a<p>Two participants (one from the standardized treatment group and one from control), described themselves as “transgender” but are reported here according to their biological gender.</p

Participant flow and reasons for dropping out throughout the trial.

<p>Abbreviations: MADRS-S: Montgomery-Åsberg Depression Rating Scale–Self-rated version; SCID: Structured Clinical Interview for DSM-IV Axis I Disorders.</p

Means, SDs and effect sizes (Cohen's d) for measures of depression, anxiety and quality of life.

<p><i>Abbreviations</i>: TA: Tailored ICBT; ST: Standardized ICBT; CO: Control group; Pre: Pre-treatment, Post: Post-treatment; FU: 6 month follow-up; BDI–II: Beck Depression Inventory-II; MADRS-S: Montgomery-Åsberg Depression Rating Scale – Self-rated version; BAI: Beck Anxiety Inventory; QOLI: Quality of Life Inventory.</p

The proportion of participants reaching recovery and clinical global improvement.

<p><i>Abbreviations</i>: TA: Tailored ICBT; ST: Standardized ICBT; CO: Control group; Pre: Pre-treatment, Post: Post-treatment; FU: 6 month follow-up; CGI-I: Clinical Global Impression – Improvement Scale.</p

Hydrogenation-Induced Structure and Property Changes in the Rare-Earth Metal Gallide NdGa: Evolution of a [GaH]^2– Polyanion Containing Peierls-like Ga–H Chains

The hydride NdGaH_1+<i>x</i> (<i>x</i> ≈ 0.66) and its deuterized analogue were obtained by sintering the Zintl phase NdGa with the CrB structure in a hydrogen atmosphere at pressures of 10−20 bar and temperatures near 300 °C. The system NdGa/NdGaH_1+<i>x</i> exhibits reversible H storage capability. H uptake and release were investigated by kinetic absorption measurements and thermal desorption mass spectroscopy, which showed a maximum H concentration corresponding to “NdGaH₂” (0.93 wt % H) and a two-step desorption process, respectively. The crystal structure of NdGaH_1+<i>x</i> was characterized by neutron diffraction (<i>P</i>2₁/<i>m</i>, <i>a</i> = 4.1103(7), <i>b</i> = 4.1662(7), <i>c</i> = 6.464(1) Å, β = 108.61(1)° <i>Z</i> = 2). H incorporates in NdGa by occupying two distinct positions, H1 and H2. H1 is coordinated in a tetrahedral fashion by Nd atoms. The H2 position displays flexible occupancy, and H2 atoms attain a trigonal bipyramidal coordination by centering a triangle of Nd atoms and bridging two Ga atoms. The phase stability and electronic structure of NdGaH_1+<i>x</i> were analyzed by first-principles DFT calculations. NdGaH1H2 (NdGaH₂) may be expressed as Nd³⁺(H1^–)­[GaH2]^2–. The two-dimensional polyanion [GaH]^2– features linear −H–Ga–H–Ga– chains with alternating short (1.8 Å) and long (2.4 Å) Ga–H distances, which resembles a Peierls distortion. H2 deficiency (<i>x</i> < 1) results in the fragmentation of chains. For <i>x</i> = 0.66 arrangements with five-atom moieties, Ga–H–Ga–H–Ga are energetically most favorable. From magnetic measurements, the Curie–Weiss constant and effective magnetic moment of NdGaH_1.66 were obtained. The former indicates antiferromagnetic interactions, and the latter attains a value of ∼3.6 μ_B, which is typical for compounds containing Nd³⁺ ions

Hydrogenation-Induced Structure and Property Changes in the Rare-Earth Metal Gallide NdGa: Evolution of a [GaH]^2– Polyanion Containing Peierls-like Ga–H Chains

The hydride NdGaH_1+<i>x</i> (<i>x</i> ≈ 0.66) and its deuterized analogue were obtained by sintering the Zintl phase NdGa with the CrB structure in a hydrogen atmosphere at pressures of 10−20 bar and temperatures near 300 °C. The system NdGa/NdGaH_1+<i>x</i> exhibits reversible H storage capability. H uptake and release were investigated by kinetic absorption measurements and thermal desorption mass spectroscopy, which showed a maximum H concentration corresponding to “NdGaH₂” (0.93 wt % H) and a two-step desorption process, respectively. The crystal structure of NdGaH_1+<i>x</i> was characterized by neutron diffraction (<i>P</i>2₁/<i>m</i>, <i>a</i> = 4.1103(7), <i>b</i> = 4.1662(7), <i>c</i> = 6.464(1) Å, β = 108.61(1)° <i>Z</i> = 2). H incorporates in NdGa by occupying two distinct positions, H1 and H2. H1 is coordinated in a tetrahedral fashion by Nd atoms. The H2 position displays flexible occupancy, and H2 atoms attain a trigonal bipyramidal coordination by centering a triangle of Nd atoms and bridging two Ga atoms. The phase stability and electronic structure of NdGaH_1+<i>x</i> were analyzed by first-principles DFT calculations. NdGaH1H2 (NdGaH₂) may be expressed as Nd³⁺(H1^–)­[GaH2]^2–. The two-dimensional polyanion [GaH]^2– features linear −H–Ga–H–Ga– chains with alternating short (1.8 Å) and long (2.4 Å) Ga–H distances, which resembles a Peierls distortion. H2 deficiency (<i>x</i> < 1) results in the fragmentation of chains. For <i>x</i> = 0.66 arrangements with five-atom moieties, Ga–H–Ga–H–Ga are energetically most favorable. From magnetic measurements, the Curie–Weiss constant and effective magnetic moment of NdGaH_1.66 were obtained. The former indicates antiferromagnetic interactions, and the latter attains a value of ∼3.6 μ_B, which is typical for compounds containing Nd³⁺ ions

Description of the self-help modules in the psychodynamic treatment.

<p>Description of the self-help modules in the psychodynamic treatment.</p

Weekly change on the Beck Depression Inventory-II during treatment and Beck Depression Inventory-II scores at each assessment point.

<p>Weekly change on the Beck Depression Inventory-II during treatment and Beck Depression Inventory-II scores at each assessment point.</p

Demographic description of the participants at randomization.

<p>Demographic description of the participants at randomization.</p

Participant flow and reasons for exclusion.

<p>Abbreviations: MADRS-S: Montgomery-Åsberg Depression Rating Scale-Self-rated version; M.I.N.I.: Mini-International Neuropsychiatric Interview; ITT: Intention-to-treat.</p