Trial Outcomes & Findings for The Relationship Between Autobiographical Memory and Motivation (NCT NCT03677635)

NCT ID: NCT03677635

Last Updated: 2025-07-18

Results Overview

A rating on a visual analogue scale assessing motivation to repeat the same activity recalled in the future. The scale is rated from 0-100 and a higher score indicated better outcome.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

31 participants

Primary outcome timeframe

Immediately after completing the intervention

Results posted on

2025-07-18

Participant Flow

A total of 31 people with a diagnosis of non-affective psychosis participated between May 2017-Feb 2018.

Participant milestones

Participant milestones
Measure
Intervention
Guided autobiographical memory recall to enhance specificity and links to the future.
Control
Recall without prompts or psychoeducation video.
Overall Study
STARTED
21
10
Overall Study
COMPLETED
21
10
Overall Study
NOT COMPLETED
0
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

The Relationship Between Autobiographical Memory and Motivation

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Intervention
n=21 Participants
Guided autobiographical memory recall to enhance specificity and links to the future.
Control
n=10 Participants
Recall without prompts or psychoeducation video.
Total
n=31 Participants
Total of all reporting groups
Age, Continuous
38.62 Years
STANDARD_DEVIATION 10.98 • n=5 Participants
41.10 Years
STANDARD_DEVIATION 9.09 • n=7 Participants
39.55 Years
STANDARD_DEVIATION 10.83 • n=5 Participants
Sex: Female, Male
Female
5 Participants
n=5 Participants
2 Participants
n=7 Participants
7 Participants
n=5 Participants
Sex: Female, Male
Male
16 Participants
n=5 Participants
8 Participants
n=7 Participants
24 Participants
n=5 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants
n=5 Participants
1 Participants
n=7 Participants
1 Participants
n=5 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
21 Participants
n=5 Participants
9 Participants
n=7 Participants
30 Participants
n=5 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
n=5 Participants
0 Participants
n=7 Participants
0 Participants
n=5 Participants
Clinical Assessment Interview for Negative Symptoms
24.1 units on a scale
STANDARD_DEVIATION 6.37 • n=5 Participants
17.1 units on a scale
STANDARD_DEVIATION 6.82 • n=7 Participants
21.73 units on a scale
STANDARD_DEVIATION 7.04 • n=5 Participants

PRIMARY outcome

Timeframe: Immediately after completing the intervention

A rating on a visual analogue scale assessing motivation to repeat the same activity recalled in the future. The scale is rated from 0-100 and a higher score indicated better outcome.

Outcome measures

Outcome measures
Measure
Intervention
n=21 Participants
Guided autobiographical memory recall to enhance specificity and links to the future.
Control
n=10 Participants
Recall without prompts or psychoeducation video.
Post-Intervention Motivation Score
81.01 units on a scale
Standard Error 4.15 • Interval 69.21 to 85.86
72.89 units on a scale
Standard Error 5.79 • Interval 65.12 to 88.38

SECONDARY outcome

Timeframe: Immediately after completing the intervention

A rating on a visual analogue scale assessing how pleasant that activity is anticipated to be if repeated. The scale is rated from 0-100 and a higher score indicated better outcome.

Outcome measures

Outcome measures
Measure
Intervention
n=21 Participants
Guided autobiographical memory recall to enhance specificity and links to the future.
Control
n=10 Participants
Recall without prompts or psychoeducation video.
Post-Intervention Anticipatory Pleasure
84.35 units on a scale
Standard Error 3.05
86.58 units on a scale
Standard Error 4.76

Adverse Events

Intervention

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Control

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Dr Clementine Edwards

King's College London

Phone: 07557866053

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place