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A Personalized Health Behavior System (FITTLESenior)

Weill Cornell Medicine (WCM) logo

Weill Cornell Medicine (WCM)

Status

Completed

Conditions

Aging
Physical Activity
Social Isolation

Treatments

Behavioral: Control Condition
Behavioral: Intervention Condition

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT03538158
R01AG053163 (U.S. NIH Grant/Contract)
1806019352

Details and patient eligibility

About

The objectives of this study are to examine the usability and efficacy, for diverse older adults, of a new tablet-based dynamic system: the Fittle Senior System (FSS) that will provide: (1) personalized behavior-change programs for improved diet and increased physical activity and (2) online social interaction and support from small teams pursuing similar goals.

The proposed study involves a two group randomized trial where participants will be randomized to the Fittle Senior System or to a paper-based psycho-educational control condition following a baseline assessment. The duration of the intervention phase will involve an active 12-week intervention phase followed by a 12-week maintenance phase. We will recruit and randomize 180 community dwelling adults aged 65+ years, who live alone and are at risk for social isolation. Participants will be assessed at baseline, 3 months post active intervention and 3 months post maintenance (6 months following active intervention) on measures of health and health behaviors, and indices of social support.

Full description

The proposed study will evaluate a new tablet-based dynamic system: the Fittle Senior System (FSS) that will provide: (1) personalized, goal-directed behavior-change programs for improved diet and increased physical activity and (2) online social interaction and support from small teams pursuing similar goals. The system builds on two technology-based systems developed by the investigative team: (1) the computer-based PRISM system (Czaja et al., 2015), designed for older populations to support social connectivity and well-being, and (2) the Fittle mobile platform (PARC) designed to support positive health behavior change through integrated online social support and personalized coaching based on artificial intelligence (AI). The Fittle program is based on Self-efficacy and Social Cognitive Theory (Bandura, 1998, 2001), Goal Setting (Locke & Latham, 2002) and the Theory of Planned Behavior (Ajzen, 1991). Fittle provides support for individuals and teams to progress through lifestyle challenges (e.g., poor eating habits, sedentary behavior), helping individuals master one health improving habit after another in a way that builds on previous achievements. Individuals choose from a variety of challenges to accomplish goals via an intelligent coaching agent and personalized, engaging user experiences. The objective is to maintain and reinforce perceived self-efficacy with daily goals that are perceived as being achievable, and to improve motivation and ability with goals that are perceived as not too easy. The program provides encouragement and social support through a team component. Thus, Fittle is designed to reinforce and build self-efficacy and positive attitudes.

Enrollment

181 patients

Sex

All

Ages

60+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • At least 60 years old
  • Speak English
  • Able to read at the 6th grade
  • Plans to remain in the area for the study duration
  • Pass TICS (Telephone Screen for Cognitive Status)

Exclusion criteria

  • Cognitively impaired
  • Visual or hearing impairment
  • Actively engaged in structured physical exercise regularly
  • Health conditions/illness that would affect participation

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

181 participants in 2 patient groups, including a placebo group

Intervention condition - Fittle Senior
Experimental group
Description:
Participants will have access to the Fittle Senior System which will provide guided exercises and social support.
Treatment:
Behavioral: Intervention Condition
Control condition - paper and pencil
Placebo Comparator group
Description:
Participants will have a written booklet with exercises that they may do it on their own.
Treatment:
Behavioral: Control Condition

Trial documents
1

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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