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Tablet-based Cognitive Behavioral Intervention for Older Adults With Arthritis Fatigue

Tablet-based Cognitive Behavioral Intervention: Comparison of Group vs. Individual CBT Education

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04792853
Enrollment
40
Registered
2021-03-11
Start date
2021-01-21
Completion date
2023-04-30
Last updated
2023-05-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arthritis, Fatigue

Keywords

arthritis, fatigue, cognitive behavioral therapy, group education, older adults, tablet, simple walking

Brief summary

The purpose of this project is to pilot test a long-term effect of Tab-G (tablet-based cognitive behavioral group education intervention). The investigators will evaluate the effect of Tab-G, relative to usual care group, on (a) daily steps, (b) fatigue level, (c) self-efficacy and (d) quality of life. Tab-G participants will receive 4 weekly CBT-based group education focusing on shared goal setting and mutual reinforcement in a group with 5 members. The outcomes will be measured baseline, week 4 (intervention completion) and week 8 (follow-up). The investigators hypothesize that older adults receiving Tab-G will have greater improvements on outcomes compared to those receiving usual care at week 4, the intervention completion and at week 8 follow-up.

Interventions

BEHAVIORALTab-G

Participants receive a tablet preloaded with Tab-G application and an accelerometer.

Sponsors

University of Massachusetts, Amherst
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

The study uses an experimental pre- and post-test repeated measures design. Those satisfying the inclusion and exclusion criteria are randomly assigned to the intervention (Tab-G, n=20) or comparison group (n=20).

Eligibility

Sex/Gender
ALL
Age
55 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. diagnosis of osteoarthritis or rheumatoid arthritis; 2. presence of greater than minimal fatigue scoring ≥13 (T-score\>55) on the Patient Reported Outcomes Measurement Information System (PROMIS) Short Form (SF) v1.0-Fatigue 6a; and 3. having Wi-Fi at home

Exclusion criteria

1. currently engaging in regular exercise; 2. non-ambulatory or presence of a condition that would limit the ability to walk (e.g., foot deformity, lower extremity joint surgery in past 6 months, stroke, severe chronic obstructive pulmonary disease, etc.); and 3. delirium, dementia, or any conditions indicating deteriorating cognitive status as determined by the Mini-Cog.

Design outcomes

Primary

MeasureTime frameDescription
daily steps24 hoursdaily step counts measured by an accelerometer
BRICS NINR PROMIS Fatigue Short Form 6apast 1 weekself-reported fatigue scale measuring both the experience of fatigue and the interference of fatigue on daily activities. Scores can range from 6 to 30, with higher scores indicating greater fatigue.
Self-Efficacy for Managing Chronic Disease 6-Item Scale24 hoursself-reported self-efficacy scale. Scores can range from 6 to 60, with higher scores indicating higher self-efficacy.
Quality of Life-Rheumatoid Arthritis Scalepast 4 weeksself-reported perception of quality of life. Scores can range from 8 to 80 with higher scores indicating greater quality of life.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026