Your browser doesn't support javascript.
loading
Pilot Randomized Controlled Trial of Feasibility, Acceptability, and Preliminary Efficacy of a Web-Based Physical Activity and Sedentary Time Intervention for Survivors of Physical Inactivity-Related Cancers.
Rees-Punia, Erika; Leach, Corinne R; Westmaas, J Lee; Dempsey, Lauren F; Roberts, Amelia M; Nocera, Joe R; Patel, Alpa V.
Afiliación
  • Rees-Punia E; Department of Population Science, American Cancer Society, Atlanta, GA, USA. Erika.rees-punia@cancer.org.
  • Leach CR; Department of Population Science, American Cancer Society, Atlanta, GA, USA.
  • Westmaas JL; Department of Population Science, American Cancer Society, Atlanta, GA, USA.
  • Dempsey LF; Department of Population Science, American Cancer Society, Atlanta, GA, USA.
  • Roberts AM; Department of Population Science, American Cancer Society, Atlanta, GA, USA.
  • Nocera JR; Departments of Neurology and Rehabilitation Medicine, Emory University, Atlanta, GA, USA.
  • Patel AV; Center for Visual and Neurocognitive Rehabilitation, Atlanta, GA, USA.
Int J Behav Med ; 29(2): 220-229, 2022 Apr.
Article en En | MEDLINE | ID: mdl-33954891
ABSTRACT

BACKGROUND:

This pilot study explored the feasibility, acceptability, and usability of a web-based intervention for survivors of physical inactivity-related cancers through a two-arm, 12-week randomized controlled trial. Secondarily, this study tested the change in physical activity (PA) and sedentary time with intervention exposure.

METHODS:

Prior to randomization to the intervention (n = 45) or behavior "as usual" wait-listed control (n = 40) groups, participants completed baseline surveys and an accelerometer protocol. The intervention focused on increasing PA and decreasing sedentary time through social cognitive theory techniques. Follow-up acceptability/usability surveys (intervention group only) and accelerometers were sent after the intervention period. Information on intervention completion, adverse events, and user statistics were collected to determine feasibility. Median login time and mean acceptability/usability scores were calculated.

RESULTS:

Participants (mean age = 60 ± 7 years) included female (n = 80, 94%) and male survivors of breast (82%), colon (6%), endometrial (6%), bladder (4%), and kidney (2%) cancer. Seventy-eight (91.7%) participants returned partially or fully complete post-intervention data. There were no reported injuries or safety concerns. Intervention participants logged into the website for a total of 95 min (Q1, Q3 = 11, 204). System usability scores (72 ± 3) indicated above average usability of the website. Changes in time spent active and sedentary were not statistically significantly different between groups (p = 0.45), but within-group changes suggested intervention group participants spent more time active and less time sedentary after the intervention.

CONCLUSION:

Results of this pilot study suggest its feasibility and acceptability for survivors of several inactivity-related cancers. Additional research to determine long-term efficacy is warranted. This low-cost online-only intervention has the potential to have a very broad reach. TRIAL REGISTRATION Clinical Trials Number NCT03983083. Date registered June 12th, 2019.
Asunto(s)
Palabras clave

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Conducta Sedentaria / Neoplasias Tipo de estudio: Clinical_trials / Guideline Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Behav Med Asunto de la revista: CIENCIAS DO COMPORTAMENTO Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Conducta Sedentaria / Neoplasias Tipo de estudio: Clinical_trials / Guideline Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Behav Med Asunto de la revista: CIENCIAS DO COMPORTAMENTO Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos