Evidence map›Paper›PMID 42312185›Full record

ArticleSSM. Mental health2026

The paradox of action: Trajectories in distress, meaning, and gene regulation following self-directed activist engagement among Black women.

Taylor A Geyton, Steven W Cole

Abstract read
In one paragraph

Article in SSM. Mental health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Taylor A GeytonSan Diego State University, 5500 Campanille Dr., San Diego, CA, 92181, USA.ORCID 0000-0003-0076-5540
Steven W ColeUniversity of California Los Angeles, School of Medicine, 10833 Le Conte Ave, Los Angeles, CA, 90095, USA.

Funding

EXITO: Enhancing Cross-disciplinary Infrastructure and Training at OregonRL5GM118963 · NIGMS · PORTLAND STATE UNIVERSITY · PI KELLER, THOMAS E · 2015 to 2023
$11.9M
Phase II of BUILDing SCHOLARS - Research Enrichment CoreRL5GM118969 · NIGMS · UNIVERSITY OF TEXAS EL PASO · PI ALEY, STEPHEN B, BOLAND, THOMAS · 2015 to 2023
$7.4M
NIGMS NIH HHS RL5 GM118963NIGMS NIH HHS RL5 GM118969
6 · The paper itself

Abstract

Background: Black women have a long history of engaging in activism and community advocacy as both a political imperative and a survival strategy (Hill Collins, 2000; Ransby, 2003). Activism may confer psychological benefits such as increased meaning in life, identity affirmation, and social connection (Hope et al., 2019; Klar and Kasser, 2009); simultaneously, activism can involve sustained stress exposure, burnout, and heightened vulnerability to surveillance and (re)traumatization (Gorski, 2019). Biological indicators offer one avenue for examining how social conditions are embodied particularly when psychosocial experiences involve chronic threat, vigilance, and cumulative stress exposure. Given growing attention to activism as a health-relevant practice, this study is framed though an intersectional and critical medical anthropology lens to explore how activism may relate to both psychosocial and biological stress processes among Black women. Methods: Using an embedded mixed-methods pilot design, this study evaluated the feasibility of assessing psychosocial indicators and the Conserved Transcriptional Response to Adversity (CTRA) at baseline (T1) and ~2-month follow-up (T2) during a self-selected intentional activism period among Black women, with baseline semi-structured interviews contextualizing interpretation of T1→T2 patterns. Participants (N = 29; M age = 39.4 years, SD = 11.7; range = 21-63) completed online surveys, a baseline interview, and coached dried blood spot (DBS) collection at T1, then completed follow-up surveys and DBS collection at T2. Analyses followed a three-part workflow: (1) feasibility metrics (enrollment/retention and useable DBS returns), (2) within-person quantitative change (paired-samples t tests for psychosocial measures; mixed-effects linear models of a 53-gene CTRA set), and (3) thematic analysis of baseline interviews with integration via joint display (convergence/complementarity/divergence). Results: Procedures supported remote biobehavioral assessment; useable DBS/CTRA data were available for most participants (T1 n = 28; T2 n = 27). Psychosocial scores decreased from T1 to T2 for psychological distress, activist orientation, and meaning in life (presence and search), with activist identity/commitment also decreasing but not reaching conventional thresholds. At the sample level, mean CTRA showed no net change from T1 to T2; however, within-person increases in activist identity/commitment and increases in search for meaning were associated with more favorable CTRA change. Baseline qualitative themes (Activism's Paradox; Identity Dialectics; Resistance and Restoration; Community-Rooted Well-being) highlighted co-occurring strain, meaning, identity negotiation under misogynoir, and relational coping infrastructure. Conclusion: Findings support feasibility and provide hypothesis-generating evidence that biobehavioral responses may be contingent on identity and meaning processes rather than uniform mean shifts in a heterogeneous activism window.

Identifiers

PMID42312185
PMCPMC13271653

What Socratic holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.