The Scleroderma Patient-centered Intervention Network Self-Management (SPIN-SELF) Program: protocol for a two-arm parallel partially nested randomized controlled feasibility trial with progression to full-scale trial
dc.contributor.author | Nordlund, Julia | |
dc.contributor.author | Henry, Richard S. | |
dc.contributor.author | Kwakkenbos, Linda | |
dc.contributor.author | Carrier, Marie-Eve | |
dc.contributor.author | Levis, Brooke | |
dc.contributor.author | Nielson, Warren R. | |
dc.contributor.author | Bartlett, Susan J. | |
dc.contributor.author | Dyas, Laura | |
dc.contributor.author | Tao, Lydia | |
dc.contributor.author | Fedoruk, Claire | |
dc.contributor.author | Nielsen, Karen | |
dc.contributor.author | Hudson, Marie | |
dc.contributor.author | Pope, Janet | |
dc.contributor.author | Frech, Tracy | |
dc.contributor.author | Gholizadeh, Shadi | |
dc.contributor.author | Johnson, Sindhu R. | |
dc.contributor.author | Piotrowski, Pamela | |
dc.contributor.author | Jewett, Lisa R. | |
dc.contributor.author | Gordon, Jessica | |
dc.contributor.author | Chung, Lorinda | |
dc.contributor.author | Bilsker, Dan | |
dc.contributor.author | Levis, Alexander W. | |
dc.contributor.author | Turner, Kimberly A. | |
dc.contributor.author | Cumin, Julie | |
dc.contributor.author | Welling, Joep | |
dc.contributor.author | Fortuné, Catherine | |
dc.contributor.author | Leite, Catarina | |
dc.contributor.author | Gottesman, Karen | |
dc.contributor.author | Sauve, Maureen | |
dc.contributor.author | Rodríguez-Reyna, Tatiana S. | |
dc.contributor.author | Larche, Maggie | |
dc.contributor.author | van Breda, Ward | |
dc.contributor.author | Suarez-Almazor, Maria E. | |
dc.contributor.author | Wurz, Amanda | |
dc.contributor.author | Culos-Reed, Nicole | |
dc.contributor.author | Malcarne, Vanessa L. | |
dc.contributor.author | Mayes, Maureen D. | |
dc.contributor.author | Boutron, Isabelle | |
dc.contributor.author | Mouthon, Luc | |
dc.contributor.author | Benedetti, Andrea | |
dc.contributor.author | Thombs, Brett D. | |
dc.date.accessioned | 2021-11-28T01:02:31Z | |
dc.date.available | 2021-11-28T01:02:31Z | |
dc.date.issued | 2021-11-27 | |
dc.date.updated | 2021-11-28T01:02:30Z | |
dc.description.abstract | Abstract Background Systemic sclerosis (scleroderma; SSc) is a rare autoimmune connective tissue disease. We completed an initial feasibility trial of an online self-administered version of the Scleroderma Patient-centered Intervention Network Self-Management (SPIN-SELF) Program using the cohort multiple randomized controlled trial (RCT) design. Due to low intervention offer uptake, we will conduct a new feasibility trial with progression to full-scale trial, using a two-arm parallel, partially nested RCT design. The SPIN-SELF Program has also been revised to include facilitator-led videoconference group sessions in addition to online material. We will test the group-based intervention delivery format, then evaluate the effect of the SPIN-SELF Program on disease management self-efficacy (primary) and patient activation, social appearance anxiety, and functional health outcomes (secondary). Methods This study is a feasibility trial with progression to full-scale RCT, pending meeting pre-defined criteria, of the SPIN-SELF Program. Participants will be recruited from the ongoing SPIN Cohort ( http://www.spinsclero.com/en/cohort ) and via social media and partner patient organizations. Eligible participants must have SSc and low to moderate disease management self-efficacy (Self-Efficacy for Managing Chronic Disease (SEMCD) Scale score ≤ 7.0). Participants will be randomized (1:1 allocation) to the group-based SPIN-SELF Program or usual care for 3 months. The primary outcome in the full-scale trial will be disease management self-efficacy based on SEMCD Scale scores at 3 months post-randomization. Secondary outcomes include SEMCD scores 6 months post-randomization plus patient activation, social appearance anxiety, and functional health outcomes at 3 and 6 months post-randomization. We will include 40 participants to assess feasibility. At the end of the feasibility portion, stoppage criteria will be used to determine if the trial procedures or SPIN-SELF Program need important modifications, thereby requiring a re-set for the full-scale trial. Otherwise, the full-scale RCT will proceed, and outcome data from the feasibility portion will be utilized in the full-scale trial. In the full-scale RCT, 524 participants will be recruited. Discussion The SPIN-SELF Program may improve disease management self-efficacy, patient activation, social appearance anxiety, and functional health outcomes in people with SSc. SPIN works with partner patient organizations around the world to disseminate its programs free-of-charge. Trial registration ClinicalTrials.gov NCT04246528 . Registered on 27 January 2020 | |
dc.identifier.citation | Trials. 2021 Nov 27;22(1):856 | |
dc.identifier.doi | https://doi.org/10.1186/s13063-021-05827-z | |
dc.identifier.uri | http://hdl.handle.net/1880/114146 | |
dc.identifier.uri | https://doi.org/10.11575/PRISM/45671 | |
dc.language.rfc3066 | en | |
dc.rights.holder | The Author(s) | |
dc.title | The Scleroderma Patient-centered Intervention Network Self-Management (SPIN-SELF) Program: protocol for a two-arm parallel partially nested randomized controlled feasibility trial with progression to full-scale trial | |
dc.type | Journal Article |