“…For a more detailed discussion on reducing participants' vulnerability to violence or distress from research participation please see: Ahlin (2019) [89], Kyegombe et al (2019) [146], and Pickles (2020) [83] for recommendations on obtaining assent from minors in vulnerable positions, Ahlin (2019) [89] and Dehghan & Wilson (2018) [88] for recommendations on handling consent or asset when potential participants may feel pressured to participate, Kimberg (2018) [91] and Sullivan & Cain (2004) [43] for recommendations pertaining to domestic violence, Allden et al (2009) [51] for recommendations pertaining to political violence and stigmatization threats, Amin and Garcia-Moreno (2018) [147] for recommendations pertaining to disclosure of sexual abuse, and Linabary & Corple (2019) [85] for recommendations concerning online research and privacy. Recommendations for minimizing the possibility of harm from data collection distress included providing resources for participants through accountable, acceptable, and available quality referrals (either through lists or proactive referrals) [27,31,51,72,73,86,92,[94][95][96], and monitoring participants' emotional well-being during and following data collection [30,44,71,73,75,79,82,97].…”